DDX42


This analysis report summarizes DDX42 eCLIP data from ENCODE. The current tab provides an overview of the results, and the other tabs list identified peaks and motifs.

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Experiment Summary


Experiment ID File ID Sample Antibody source Antibody ID Antibody lot Release date Laboratory Number of peaks
ENCSR576SHTENCFF399GGHK562Bethyl LabsA303-353A12015-07-15Gene Yeo, UCSD110

DDX42 Peak Assignments


The following plots show the assignment of peaks into different genic features:

Introns contain other subdivisions, please see the subsequent plot for a breakdown of those features.

This plot is interactive. You can hover over the bars to see the percentage and number of identified peaks. You can select which features to show by toggling the region names in the legend, and you can download the plot by moving your mouse to the top of the plot and clicking on the camera icon.

DDX42 Intron Assignments


The following plots show the assignment of peaks into different intronic features:

  •  5’ splice site: the peak is within the first 100 bp of an intron (5’ to 3’ direction
  •  3’ splice site: the peak is within the last 100 bp of an intron (5’ to 3’ direction)
  •  Proximal intron: the peak is within 100 bp to 500 bp of the nearest exon
  •  Distal intron: greater than 500 bp away from the nearest exon

This plot is interactive. You can hover over the bars to see the percentage and number of identified peaks. You can select which features to show by toggling the region names in the legend, and you can download the plot by moving your mouse to the top of the plot and clicking on the camera icon.

DDX42 Motifs


The following plot shows a summary of the top five motifs by significance in each experiment. Motifs were detected with varying length parameters, you may observe a similar motif with different number of bases included multiple times. A motif present in more peaks and with a higher significance will be in the upper right quadrant of the plot, while the lower left quadrant has motifs that are less significant and in fewer peaks.

This plot is interactive. You can hover over the bars to see the percentage and number of identified peaks. You can select which features to show by toggling the region names in the legend, and you can download the plot by moving your mouse to the top of the plot and clicking on the camera icon.

No significant motif were identified


The following table contains called DDX42 peaks. To identify peaks, clusters (regions of read enrichment) in the immunoprecipitated (IP) samples were found using the peak calling tool CLIPper. To account for background signal, a cluster was identified as a peak if the log2 fold enrichment over input was ≥ 3 and the p-value ≤ 0.001.

Peaks were annotated using transcript information from GENCODE. Each annotated peak is labeled with specific annotation feature types, first split by coding and non-coding transcripts, then by transcript regions, and then by intron/exon proximity regions. For overlapping transcript regions, the following hierarchy is used to label the region: coding sequence (CDS), 5’ or 3’ untranslated region (UTR), intron, non-coding exon, then non-coding intron. For example, if a peak is in the 5’ UTR of one transcript that overlaps an intron of another transcript, the peak region will be labeled as 5’ UTR. All gene annotations are from GENCODE release v41.

The following columns are included in the table:

  •  Chromosome: chromosome where the peak is located.
  •  Peak start: start coordinate for the peak.
  •  Peak stop: stop coordinate for the peak.
  •  Strand: strand of DNA where the peak was called.
  •  -log10(p-value): significance of the cluster call by CLIPper. Values are log transformed so a larger number indicates a greater significance.
  •  log2(fold change): log transformed fold enrichment of the IP signal over a matched input.
  •  Gene name: name (symbol) of the gene that overlaps with the peak.
  •  Ensembl ID: unique identifer of the gene that overlaps with the peak.
  •  Feature: which part of the listed gene overlaps with the peak.

Please note, this table is interactive. You can search for specific genes or features, and can sort the table by any of the columns.

ENCSR576SHT (K562) Peaks


Chromosome Peak start Peak stop Strand -log10(p-value) log2(fold change) Gene name Ensembl ID Feature
chr2131,281,158131,281,222+6.1533.030PLEKHB2ENSG00000115762.17Distal intron
chr2249,644,37449,644,425-5.3023.603MIR3667HGENSG00000188511.14ncRNA
chr76,026,5966,026,659-4.6644.184EIF2AK1ENSG00000086232.135' splice site
chr135,182,12735,182,183-10.2733.044SFPQENSG00000116560.12ncRNA
chr543,483,68043,483,813-4.5963.442TMEM267ENSG00000151881.155' splice site
chr39,434,7169,434,767+5.5183.369SETD5ENSG00000168137.203' splice site
chr205,610,6625,610,795-4.5963.623GPCPD1ENSG00000125772.145' splice site
chr4173,333,715173,333,852-7.1103.307HMGB2ENSG00000164104.123' splice site
chr19803,508803,559+5.9823.330PTBP1ENSG00000011304.223' splice site
chr218,218,7408,218,832+400.0004.994ENSG00000278996ENSG00000278996.1ncRNA
chr2043,459,04343,459,085+10.8366.223SRSF6|ENSG00000288000ENSG00000288000.1||ENSG00000124193.16Distal intron
chr265,269,30165,269,355+23.4233.178ACTR2ENSG00000138071.153' UTR
chr2131,211,296131,211,381+4.1163.519POTEEENSG00000188219.16Proximal intron
chr643,777,83043,777,875+4.1863.114VEGFAENSG00000112715.26Proximal intron
chr75,530,1655,530,238-30.7293.015ACTBENSG00000075624.17Proximal intron
chr1590,911,27890,911,333+4.6644.060MAN2A2ENSG00000196547.155' splice site
chr1780,337,44180,337,546+5.5743.810RNF213ENSG00000173821.203' splice site
chr1172,703,40172,703,415-3.9373.342ARAP1ENSG00000186635.155' UTR
chr1172,703,39572,703,401-3.5213.020ARAP1ENSG00000186635.155' UTR
chr539,073,97039,074,059-6.4385.305RICTORENSG00000164327.135' splice site
chr2043,458,88643,458,938+11.7444.792SRSF6|ENSG00000288000ENSG00000288000.1||ENSG00000124193.16Proximal intron
chr1068,338,04768,338,098+5.4704.138HNRNPH3ENSG00000096746.185' splice site
chr643,770,83643,770,861+3.6433.603VEGFAENSG00000112715.26CDS
chr7139,371,549139,371,602+3.3503.374LUC7L2ENSG00000146963.185' splice site
chr11126,268,043126,268,092-3.6623.915SRPRAENSG00000182934.12CDS
chr192,270,1102,270,139+4.5773.927OAZ1ENSG00000104904.12Proximal intron
chr347,853,26847,853,345-6.0713.823MAP4ENSG00000047849.22CDS
chr1688,658,72988,658,795-6.8764.459MVDENSG00000167508.123' splice site
chr1151,400,930151,401,022+5.1734.247PSMB4ENSG00000159377.115' splice site
chr1782,092,31682,092,341-4.9463.176FASNENSG00000169710.9Proximal intron
chr632,972,96932,973,062+8.6633.285BRD2ENSG00000204256.145' splice site
chr3100,709,925100,710,044+3.7544.915TFGENSG00000114354.155' UTR
chr2139,348,66039,348,700-5.3023.652HMGN1ENSG00000205581.113' splice site
chr296,869,73796,869,802-6.2034.638SEMA4CENSG00000168758.115' splice site
chr12123,510,180123,510,374-6.5723.906RILPL1ENSG00000188026.13Distal intron
chr1165,427,39365,427,418+27.5603.027NEAT1ENSG00000245532.11ncRNA
chr10123,154,671123,154,776+5.6864.181BUB3ENSG00000154473.18Proximal intron
chr1912,938,91912,938,955+5.5183.546CALRENSG00000179218.15Proximal intron
chr1768,035,90668,035,962+5.9364.369KPNA2ENSG00000182481.105' UTR
chr158,781,58558,781,659-9.1883.257JUNENSG00000177606.83' UTR
chr1776,736,73176,736,787-4.8453.052hsa-mir-636MI0003651miRNA
chr1256,161,18456,161,240+3.6433.636MYL6ENSG00000092841.193' UTR
chr1775,779,42875,779,490-8.1433.264H3-3BENSG00000132475.105' splice site
chr632,974,81432,974,872+7.5854.473BRD2ENSG00000204256.145' splice site
chr296,894,25296,894,353-16.6633.862FAM178BENSG00000168754.15Proximal intron
chr162,768,4172,768,450+4.5963.768SRRM2ENSG00000167978.17Proximal intron
chr631,535,75231,535,794-4.6644.145DDX39BENSG00000198563.14Proximal intron
chr11,393,1641,393,217-5.5743.649CCNL2ENSG00000221978.13Proximal intron
chr7100,882,406100,882,458+5.9823.132SRRTENSG00000087087.20Proximal intron
chr1226,071,347226,071,373+4.6644.014H3-3AENSG00000163041.13CDS
chr1781,936,79681,936,867-5.1734.167PYCR1ENSG00000183010.17CDS
chr1628,826,25128,826,287+5.1943.374ATXN2LENSG00000168488.19CDS
chr1764,505,55464,505,595-4.7703.188DDX5ENSG00000108654.16CDS
chr238,750,59938,750,675-5.7543.137SRSF7ENSG00000115875.19Proximal intron
chr1166,617,13566,617,213+5.9883.082RBM14|RBM14-RBM4ENSG00000248643.5||ENSG00000239306.55' splice site
chr499,949,90799,949,988-6.2034.358H2AZ1ENSG00000164032.12Proximal intron
chr1244,863,183244,863,239-5.5183.661HNRNPUENSG00000153187.20Proximal intron
chr1220,210,626220,210,686-3.6633.256RAB3GAP2ENSG00000118873.17Proximal intron
chr1688,732,81588,732,858-4.1163.076PIEZO1ENSG00000103335.223' splice site
chr1743,290,29243,290,297-41.1405.476U2ENSG00000274452.1ncRNA
chr1743,290,30743,290,345-44.8085.337U2ENSG00000274452.1ncRNA
chr1743,290,29743,290,307-43.3145.284U2ENSG00000274452.1ncRNA
chr1244,863,063244,863,120-8.5613.497HNRNPUENSG00000153187.205' UTR
chr1743,387,34343,387,414-8.3044.793RNU2-4P|LINC00910ENSG00000188825.16||ENSG00000277084.1ncRNA
chr1070,170,23670,170,309-4.5963.582SAR1AENSG00000079332.15Proximal intron
chrX154,399,428154,399,473+13.0193.473RPL10ENSG00000147403.185' splice site
chr1910,296,48310,296,579+14.4923.365ICAM5ENSG00000105376.5CDS
chr643,778,38543,778,439+7.0583.717VEGFAENSG00000112715.263' splice site
chrX12,976,42212,976,478+5.0823.549TMSB4XENSG00000205542.115' splice site
chr218,401,8178,401,857+63.3998.319ENSG00000280441ENSG00000280441.3ncRNA
chr218,401,7798,401,817+64.4308.302ENSG00000280441ENSG00000280441.3ncRNA
chr218,397,5648,397,665+5.0823.720ENSG00000280441ENSG00000280441.3ncRNA
chrX71,366,52271,366,673+10.8563.485TAF1ENSG00000147133.175' splice site
chr2177,212,915177,212,972+4.7703.188hsa-mir-4444-1MI0016787miRNA
chr1747,975,78547,975,867+10.2493.129CDK5RAP3ENSG00000108465.153' splice site
chr983,979,63483,979,712-7.2135.330HNRNPKENSG00000165119.21Proximal intron
chr470,982,15170,982,208+8.6923.671MOB1BENSG00000173542.93' UTR
chr192,270,2152,270,279+15.6284.683OAZ1ENSG00000104904.12Proximal intron
chr2043,458,56043,458,614+16.7143.789ENSG00000288000|SRSF6ENSG00000124193.16||ENSG00000288000.15' splice site
chr1162,841,75262,841,795-22.6007.060WDR74ENSG00000133316.165' UTR
chr2250,443,78650,443,900+4.5963.582PPP6R2ENSG00000100239.16CDS
chrX71,541,78171,541,860+5.5743.773OGTENSG00000147162.15Distal intron
chr1911,089,70711,089,801+6.5723.906LDLRENSG00000130164.145' splice site
chr1918,571,93218,572,006+4.5493.853UBA52ENSG00000221983.85' UTR
chr2249,639,30249,639,370-4.5963.538MIR3667HGENSG00000188511.14ncRNA
chr426,857,78526,857,876+3.5313.445STIM2ENSG00000109689.205' splice site
chr1910,296,35710,296,411+8.1433.419ICAM5ENSG00000105376.5CDS
chr19806,898806,951+6.1533.067PTBP1ENSG00000011304.22Proximal intron
chr1590,912,29290,912,366+6.5193.123MAN2A2ENSG00000196547.155' splice site
chr162,760,0532,760,125+16.0574.343SRRM2ENSG00000167978.17Proximal intron
chr192,270,7082,270,716+4.1604.395OAZ1ENSG00000104904.125' splice site
chr1555,853,47555,853,490-6.4386.058NEDD4ENSG00000069869.17Distal intron
chr1555,853,46555,853,475-6.4386.045NEDD4ENSG00000069869.17Distal intron
chr1555,853,45955,853,465-3.2294.858NEDD4ENSG00000069869.17Distal intron
chr482,428,94382,429,071-7.0773.151HNRNPDLENSG00000152795.18Proximal intron
chr39,434,2859,434,328+4.5963.491SETD5ENSG00000168137.20CDS
chr2030,723,85130,723,930-4.1604.115ANKRD20A21PENSG00000277112.3ncRNA
chr75,529,8265,529,892-15.6203.037ACTBENSG00000075624.175' UTR
chr11,320,7951,320,876-4.7703.328INTS11ENSG00000127054.22Proximal intron
chr424,537,11224,537,170-5.4443.086DHX15ENSG00000109606.13CDS
chr1162,841,71762,841,752-55.9144.728WDR74ENSG00000133316.165' UTR
chr1628,155,71128,155,781-4.2844.645XPO6ENSG00000169180.12Proximal intron
chr132,366,69232,366,758-4.5963.699BSDC1ENSG00000160058.193' UTR
chr1764,505,98164,506,022-5.5743.693DDX5ENSG00000108654.165' splice site
chr1948,619,02648,619,068-4.8184.895RPL18ENSG00000063177.135' UTR
chr1590,911,08090,911,147+6.2295.084MAN2A2ENSG00000196547.153' splice site
chr643,778,25743,778,303+5.9823.801VEGFAENSG00000112715.26Proximal intron
chr643,778,14743,778,242+23.4853.640VEGFAENSG00000112715.26Proximal intron
chr643,778,11943,778,147+9.2533.452VEGFAENSG00000112715.26Proximal intron
chr643,778,07043,778,119+7.3363.226VEGFAENSG00000112715.26Proximal intron

The following table contains identified motifs, where a motif is a short sequence of nucleotides that is significantly enriched in called peaks. Motifs were identified using HOMER's findMotifsGenome.pl tool. Motifs were called at multiple lengths, and results from all examined lengths are aggregated in the table.

The following columns are included in the table:

  •  Motif: logo plot for the identified motif.
  •  IUPAC: sequence of motif in IUPAC code.
  •  Motif length: length of the called motif.
  •  P-value: Significance of the called motif.
  •  -log10(p-value): log transformed significance, a larger number indicates a greater significance.
  •  % Peaks: percent of examined peaks with the identified motif.
  •  % Background: percent of non-peak background regions with the motif.

Please note, this table is interactive. You can search for specific sequences, and can sort the table by any of the columns. The search buttons at thr bottom of the table allow for specific filtering by sequence or motif length.

ENCSR576SHT (K562) Motifs


No significant motif were identified