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

TagContent
EnhancerAtlas ID
HS091-17018 
Organism
Homo sapiens 
Tissue/cell
HepG2 
Coordinate
chr16:30411430-30413730 
Target genes
Number: 57             
NameEnsembl ID
AC009133.19ENSG00000262323
QPRTENSG00000103485
KIF22ENSG00000079616
MAZENSG00000103495
AC009133.15ENSG00000259952
AC009133.14ENSG00000238045
MVPENSG00000013364
CTDENSG00000214725
CDIPTENSG00000103502
SEZ6L2ENSG00000174938
ASPHD1ENSG00000174939
KCTD13ENSG00000174943
TMEM219ENSG00000149932
TAOK2ENSG00000149930
INO80EENSG00000169592
HIRIP3ENSG00000149929
DOC2AENSG00000149927
FAM57BENSG00000149926
ALDOAENSG00000149925
PPP4CENSG00000149923
YPEL3ENSG00000090238
GDPD3ENSG00000102886
MAPK3ENSG00000102882
CORO1AENSG00000102879
RP11ENSG00000261416
SLX1AENSG00000132207
SULT1A3ENSG00000213599
BOLA2BENSG00000169627
CD2BP2ENSG00000169217
TBC1D10BENSG00000169221
ZNF48ENSG00000180035
SEPT1ENSG00000180096
ZNF771ENSG00000179965
DCTPP1ENSG00000179958
SEPHS2ENSG00000179918
ITGALENSG00000005844
ZNF768ENSG00000169957
AC002310.12ENSG00000235560
AC002310.11ENSG00000261459
AC002310.10ENSG00000260494
AC002310.13ENSG00000260869
ZNF764ENSG00000169951
AC002310.7ENSG00000239791
ZNF785ENSG00000197162
AC002310.17ENSG00000261588
ZNF689ENSG00000156853
PRR14ENSG00000156858
FBRSENSG00000156860
SRCAPENSG00000080603
SNORA30ENSG00000206755
PHKG2ENSG00000156873
RNF40ENSG00000103549
ZNF629ENSG00000102870
MIR762ENSG00000211591
SETD1AENSG00000099381
HSD3B7ENSG00000099377
STX4ENSG00000103496
TF binding sites/motifs
Number: 11             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
IRF1MA0050.2chr16:30412594-30412615GATTTCTTTCTTTTTCTTTTT+6.53
JUN(var.2)MA0489.1chr16:30411755-30411769GGGAAATGAGTCAT+6.48
RFX1MA0509.2chr16:30411626-30411642TGTTGCTATGGCGACG+6.47
RFX1MA0509.2chr16:30411626-30411642TGTTGCTATGGCGACG-6.47
RFX2MA0600.2chr16:30411626-30411642TGTTGCTATGGCGACG-6.61
RFX2MA0600.2chr16:30411626-30411642TGTTGCTATGGCGACG+6.76
RFX5MA0510.2chr16:30411626-30411642TGTTGCTATGGCGACG-6.54
RFX5MA0510.2chr16:30411626-30411642TGTTGCTATGGCGACG+6.62
ZBTB33MA0527.1chr16:30412036-30412051TTCTCGCGAGATCGT+6.36
ZNF263MA0528.1chr16:30411592-30411613CAAGGAGGAGGAAGAGGGGGC+6.2
ZfxMA0146.2chr16:30412855-30412869CCCGCCTCGGCCTC+6.01
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr163041289930413374
Number: 1             
IDChromosomeStartEnd
GH16I030398chr163040981530413617
Enhancer Sequence
TCAGCGGCTT TCTAGCTCCG ACGTCTGGTT CAAAAACGGC CGCCAGCTCC ATCAGCCGAT 60
GCCCCAGGCC TGAGGTCTGG CTGCCCGCAG GCACCACCTA CGCCACAGCA TCCAGCGCGA 120
CCCTTAAAAG GAAAACCGCG CGGCGCTGCA GAGACAAGGC AGCAAGGAGG AGGAAGAGGG 180
GGCGTGTGGG GGGCGTTGTT GCTATGGCGA CGGCTGTCGG CGGGAGGCAG CCCACAGGTC 240
TGGAACCGGC GTGGAAAGCC CGGACGCCGG CGCGCCGCCC ACCGGGACCT GGGAAACCCG 300
ACACCCGAGA CCCTTTTTAT GCGTCGGGAA ATGAGTCATT CGGCTGCACA GCCCAAAGGG 360
AGGGCAAACG GTGCTCCTTC ACCCCCAGAA AAGCCCGCCG GATTTCCCGG CGCCCCGCGG 420
GGCCTGGGAA GCAGGTCTGC AATCCCTAGC GTTTTCACAA CCACTGGCCT GATCGGCCAG 480
GGATTAAAGA AAAAAGAAGT CCAGGGCGGT TCTCCCCGCT AAACAATGAA GGCAACGAAG 540
TACAGGGTCG CAAGTTCCCG CCCCCGGCTC TCCCCGATCT CCGTGCGGAA AGAATCCCTG 600
GACGGGTTCT CGCGAGATCG TAAGCACTGG CCTGGCTTCC CTAGAAACCG ACCAGGGCTG 660
GCTGCAGTGC GGCTCCTCCC GCTCCGCCCG CCCTTTCCAA ATTGATGCGC TCTCAAAACC 720
CTAGAACCCT GCGTTCAGGG CTGGGGCTCT TGATGGCCTG AGCGGAGCCC TTTGGGGCTT 780
CTGGAAGTTC CTTCTTGCTG GTTTTCCTAG CTCCCTTCCC TACCAGTGTG CCCTCCAAGA 840
CGACCTGCAG TGAACTTTCT TTTCTTTTTT TTTGAGACGG AGTCTCGCTC TGTCGCCCAG 900
GCTGGAGTGC AGTGGCGCGA TCTTGGCTCA CTGCAACCTC CGCCTCCCGG GTTCAAGCGA 960
TTCTCCTGCC TCAGCCTCCT GAGTAGCTGG GATTACAGGC GCGCTACCAA GCCCGGCTAA 1020
TTTTTGTATT TTTAGTAGAG ACGGAGTTTC ACCATGTTTG TCAGGCTGGT CTCGAACTCC 1080
GGACTTCGTG ATCCGCCCGC CTCAGCCTTC CAAAGTGCTG GGATTACAGG CGTGAGCCAC 1140
CGCGCCTGGC CACTTTCTTT TCTTGATTTC TTTCTTTTTC TTTTTTCTTT TTTTCTCAAG 1200
ACAGGGTCTC ACTCACTCTG TCGCCCAGGC TGGAGTGCAG TGGCAGGATC TTCGGCTCAC 1260
TGCAGCCTCC GCTCGGGTTC AAGCGATTCT CCTGCCTCAG CCTCCCTAGT AGCTGGGATT 1320
ACAGGCGTCC GCCACCGCGC CTGGCTAATT TTTTTATTTT TAGTAGAGAC GGGGTTTCAC 1380
CATGTTGGCC AGGCTGGTCT CAAACTCCTG ACCTTAGGTG ATCTGCCCGC CTCGGCCTCC 1440
CAAAGTGCTA GGATTTATAG GCATGAGCCA CCGTGCCTGG CCTGCTTTCT AAAATTACAT 1500
CTGGCCATGT CACTCCCCCA TTGAAACCCC AGTGGATCTC CACATGCTGT CCCCAAAGCC 1560
TAACTTTCAT TGGCACTCAA GCCCTTCCAT TTGTGTAGTT TCAGCCCTGG GCTCCTTAAA 1620
TGTCGTTTCT TTTACTTGGA ATGCTCCTCC ACCACTACCC ACCCCTTGTT AATCTCCTCT 1680
GTCAAAACAC CTCAAGCACT ACTTCCTCCA AGAAGCCTAC TCTGACCCTC GTCTGGGTTA 1740
GTTACAATCC CCTTCTCTGA GCAACCCGTC TCTGAGCACC TAACACATGA AGAGCTTCTT 1800
GAGGATAGTT ACTCACTCAA CAGCTGCACC TATTGTGTGC TGCATACTGG GATAGAAAGA 1860
TAAACAAGAC AAAGTCCCTG ACCTGTTTTT ATGCGGGAGA TAGACATTGA ACAAATAATT 1920
ACAAGTGAGG TGAGAAATGT CCAGCAAACC TATGAGCTGG AAAGAATCCT CTGTGATCCA 1980
AAGGCCTTTC CAGGCCAGGT GTGGCTCAGG CCTGTCATCC CAGCATTTTG AGAGGTTGAG 2040
GCAGGAGGCC AGGAGGCCAG GAGTTCGAGA CCAGCCTGGG CAACATAGTG AGACCTCTCT 2100
ACAAAAAATA CAAAAATTAG GTGGAATGCA CCTGTAGTCC CAGCAACTCA GGAGGCTGAG 2160
GTGGGAGGAT CGCTTGGCCC CAGGAAGTTG AGGCTGCAGT GAGCCATGAT CATGCCACTG 2220
CACTCCATCC TGGGCAAAAG AGCAAGATCT TGTCTCCAAA AAACAAAAAC GACCCCCGCC 2280
ACCACCAGAA AATACTGTAA 2300