EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS088-03769 
Organism
Homo sapiens 
Tissue/cell
HeLa-S3 
Coordinate
chr1:155015990-155017660 
Target genes
Number: 42             
NameEnsembl ID
UBE2Q1ENSG00000160714
ADARENSG00000160710
RP11ENSG00000250970
KCNN3ENSG00000143603
PMVKENSG00000163344
PBXIP1ENSG00000163346
PYGO2ENSG00000163348
SHC1ENSG00000160691
CKS1BENSG00000173207
FLAD1ENSG00000160688
LENEPENSG00000163352
ZBTB7BENSG00000160685
DCST2ENSG00000163354
DCST1ENSG00000163357
ADAM15ENSG00000143537
EFNA4ENSG00000243364
EFNA3ENSG00000143590
EFNA1ENSG00000169242
SLC50A1ENSG00000169241
DPM3ENSG00000179085
HMGN2P18ENSG00000223452
TRIM46ENSG00000163462
KRTCAP2ENSG00000163463
MUC1ENSG00000185499
MTX1ENSG00000173171
THBS3ENSG00000169231
GBAP1ENSG00000160766
MTX1P1ENSG00000236675
AL713999.1ENSG00000216109
GBAENSG00000177628
FAM189BENSG00000160767
SCAMP3ENSG00000116521
HCN3ENSG00000143630
CLK2ENSG00000176444
PKLRENSG00000143627
FDPSENSG00000160752
RUSC1ENSG00000160753
ASH1LENSG00000227773
snoU13ENSG00000238805
POU5F1P4ENSG00000237872
DAP3ENSG00000132676
YY1AP1ENSG00000163374
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs76735429chr1155016127hg19
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
CTCFMA0139.1chr1:155017560-155017579TCTCCACAAGAGGGCACTC+6.44
EWSR1-FLI1MA0149.1chr1:155017431-155017449GGAAGGAAGGAGGCACAG+6.04
EWSR1-FLI1MA0149.1chr1:155017427-155017445GGAGGGAAGGAAGGAGGC+7.41
FOXA1MA0148.4chr1:155016114-155016130CTTTGTTTACACAAAG-6.11
IRF1MA0050.2chr1:155016334-155016355TTTTGCTTTCATTTTCTCCTG+6.96
IRF2MA0051.1chr1:155016333-155016351ATTTTGCTTTCATTTTCT-6.01
Number of super-enhancer constituents: 5             
IDCoordinateTissue/cell
SE_27386chr1:155016985-155017672Esophagus
SE_41765chr1:155014870-155016231LNCaP
SE_41765chr1:155016299-155016775LNCaP
SE_41765chr1:155016859-155017626LNCaP
SE_50747chr1:155015129-155018108Sigmoid_Colon
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr1155016228155016595
chr1155017065155017634
Number: 1             
IDChromosomeStartEnd
GH01I155042chr1155015098155018110
Enhancer Sequence
CCATAGTCCC CACCCCAGCA GCCCCTCCTC TGCCCCGGAC TGGAGCCCTG CCCTGAGGGA 60
GGCTGTAAGG ATGGAACCCT AGCACCTATC CTCACCTCTG AATCTGAATA TTATTTACCT 120
TTGTCTTTGT TTACACAAAG TTAAAGGAAA AGTGGACATT TTGTCAGAAG AACATTACCC 180
ATGTTCCCAC TGCCTTAAAA GGCCAACCGT CTTCATTCAT CCACCTCCTT CCAGCCTTTA 240
TCCCAATACT GATTTTTTTT TTTTACGTTT AGCTTTGACT TTTGATTTTT TCTTGCCCTT 300
CATATTCCCC TTGGCTCTGA CTTTGTGCCA TTTTTATCTT TCCATTTTGC TTTCATTTTC 360
TCCTGCCTGC TGCGTTGGCA GCGACTTTCC CTCCATTTAG AACAAAGTCC TCAACCCCAC 420
CCAGCCCAGT GTCCAGCTGG GCTGCCCCGG GCCTTGCTCT GCTCTAGCTC CCCTGCTGGT 480
CTCTGGACCC TCTATTTCCC ATCTCCACTC CCAAACACCT GAGATGGGCA GGGCTTGGGT 540
GAGGGCTGCC ACAGGGCTGT TGCTCTGTCT GCCCCTATGT GGGGGGCCTA GAGTGACTGC 600
AAGTGAGTGG GTATGTGTGT ATCTAGGGCC CCATGGGAAG ACAAAGATGA AGGAGCTCTA 660
TTCCTGCCCC CAATAAGCTC ATGATCGCCA GGCATGGCGG CTCACTCCTG TAATCCCAAC 720
ATTTTGGGAA GCCGAGGTGG GAGGATGGCT TGAGTTGAGG TGTTTGAGAC CAGCCTGGGT 780
AACACAGTGA GACCTCGTCT CTACAAAAAA TGAACAAAAT CAGCCAGGTG TGGGGCACAT 840
GCCTGTAGTC CCAGCTACTT GGGAGGCTGA GGCAGGAGAA TCACTGGGAG GTCGAAGCTG 900
CAGTGAGCTG TGATTGTGCC ACTGCATTCT GCATTCCAGC CTGGTGTCAG AGTGAGAGCT 960
TGTCTCAAAA AAAAAAAAAA AAAAAAAAAG CTAATGATCT AGTTGGGATC ATGAGACACC 1020
CACAAGACAG AGATGGTTCA AGGGCCATTC TATGGATTGG CTTTTGAGAC GTGTATGGGA 1080
GCTGGGAAGG TGCCCCTTGG AAGGGCAATA ACTGGGCTCC AAATGGCCGC AGATGCGGAA 1140
CGGTGGTCAA GGAAAGAAGG GTGTCCCTTG CGTAAGGCTC CTGGTATCCA TGGGATGCAG 1200
AGGGCAGAGG CTGGCCTGGA GAACTGAAGT GGGCATGACC AGAACAGTCT GGAAAGCCCT 1260
GCAGGAAGAC CTGGAACTGG CGGTGGTGGC AAGATGGCCT CAGGAAGTCT GGAGGGAGGG 1320
CGGGAGGCCA GGCTGGGTTG GAGGTTAGGG AGCCTGGCCC GGGTAGAGCA TGGCAGGAAG 1380
ATGGCTTGAG ATGGTGGGGG AAGGGGAAAG GTGCAGCGAG GCTCAGAGCC AGCTTGTGGA 1440
GGGAAGGAAG GAGGCACAGA GTCAAAAGCT ACTTCCAGGC TTTCAAGCTG GGTGAGGTCA 1500
TGCACTGAAA GGACAGCTGG CGGGAGGGCA GGCCCTGGCT CAGGAAGCCC AGGCACCACC 1560
TCTGTGAGCC TCTCCACAAG AGGGCACTCA CAGTATGTCT TTGCACTTAC AGTAGTTTTA 1620
AAGGCAAAGA TGTGGATTTT TACAGGGCCC CAGAAGCAAT AGCATTGAAA 1670