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

TagContent
EnhancerAtlas ID
HS091-17092 
Organism
Homo sapiens 
Tissue/cell
HepG2 
Coordinate
chr16:31129210-31131500 
Target genes
Number: 44             
NameEnsembl ID
ZNF768ENSG00000169957
AC002310.17ENSG00000261588
RP11ENSG00000260113
FBRSENSG00000156860
SRCAPENSG00000080603
SNORA30ENSG00000206755
PHKG2ENSG00000156873
RNF40ENSG00000103549
C16orf93ENSG00000196118
ZNF629ENSG00000102870
MIR4519ENSG00000260083
MIR762ENSG00000211591
BCL7CENSG00000099385
CTF1ENSG00000150281
FBXL19ENSG00000099364
AC135048.13ENSG00000261487
ORAI3ENSG00000175938
SETD1AENSG00000099381
HSD3B7ENSG00000099377
STX1BENSG00000099365
STX4ENSG00000103496
AC135050.1ENSG00000232748
AC135050.5ENSG00000261124
ZNF668ENSG00000167394
ZNF646ENSG00000167395
PRSS53ENSG00000151006
VKORC1ENSG00000167397
BCKDKENSG00000103507
AC135050.2ENSG00000252809
KAT8ENSG00000103510
PRSS8ENSG00000052344
PRSS36ENSG00000178226
FUSENSG00000089280
AC106782.18ENSG00000261359
PYCARDENSG00000103490
ITGAMENSG00000169896
ARMC5ENSG00000140691
TGFB1I1ENSG00000140682
SLC5A2ENSG00000140675
AC026471.6ENSG00000260740
C16orf58ENSG00000140688
CSDAP1ENSG00000261614
KIAA0664L3ENSG00000131797
CTDENSG00000261731
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs9925964chr1631129895hg19
TF binding sites/motifs
Number: 10             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EsrraMA0592.2chr16:31129399-31129410TTGACCTTGAA-6.14
Foxd3MA0041.1chr16:31130477-31130489GTTTGTTTGTTT+6.32
KLF16MA0741.1chr16:31129234-31129245GGGGGCGGGGC-6.02
KLF5MA0599.1chr16:31129235-31129245GGGGCGGGGC-6.02
KLF5MA0599.1chr16:31129265-31129275GGGGCGGGGC-6.02
KLF5MA0599.1chr16:31129331-31129341GGGGCGGGGC-6.02
Nr2f6(var.2)MA0728.1chr16:31130689-31130704TGACCTCTTAACCTC-7.77
SP1MA0079.4chr16:31129329-31129344GAGGGGCGGGGCTTG-6.34
SP2MA0516.2chr16:31129328-31129345GGAGGGGCGGGGCTTGA-6.29
SP4MA0685.1chr16:31129327-31129344AGGAGGGGCGGGGCTTG-6.49
Number of super-enhancer constituents: 3             
IDCoordinateTissue/cell
SE_09570chr16:31122347-31132628CD14
SE_26229chr16:31128868-31132413Duodenum_Smooth_Muscle
SE_26836chr16:31128082-31131019Esophagus
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr163112961631130225
Enhancer Sequence
GGCGTGAGGG CGGGGCCCAG GGCTGGGGGC GGGGCGGAGC TCAGGGCCAG GGGGTGGGGC 60
GGGGCCTGAG GACAGGCTGT CAGTGAGGCC AAGATCCGGG GGCTGGGAGT GGAGAGGAGG 120
AGGGGCGGGG CTTGAGGAAA GAACGCCGCG TTCCGGGCGC TGAGAAACCA GCCGGGTTGT 180
GGGAGGCTGT TGACCTTGAA TTATGCCGAG CGACGCCTAC AAACCCACCG CTCAGGCCTT 240
CACCAGGATT GTTCCCATTC CACTTCCTTG CCCAGTCTTA GGCTTCATTC CTTTTTCTTG 300
CTAACGCTGC TTCCTCACCC TCTCTTGTCT CTGCGTCTTC TTTTTCCATT TGTCCCTGGC 360
AGCCATCCGC AGAGAGAAGA CCTTCCAGAA ACAACAGGCT TCCCTTTCCT AAAGTTCTGC 420
TGCCTTCTCT CATTTTCAAA ATTAACCCCA AACTCCTTAG GGTGGCATTC ATTTTTGTGA 480
CCTCTCCAGT TTCTAGCCAA CACTAGGAAA GGGCATTGCC AGGCCAGAAC ACACTGTGCC 540
CTCTGAAGAC CACACGCCCT TTACCACCTG TGCCCTTTGC TTGGAATGCT TTTTCTTCCC 600
TTTCTCCTTG TTTGCCTGCC TAGCTCCTAC TCATCCTCTT AGCTTCATAT CCTTTGTGAT 660
GTCATCCTTG ATTCCCCTTC AGGCAAAGTG AGTGGTTCCC TTCTCTATGT TCCTGCAACA 720
TTTTTTTCCT ACCTCAGTCA TAGTTTTTGT AACATTATGT TGTAATTTTC TCTCTCTGTC 780
TTCCTCCATC ATACTGGGAA CTTCTGGAGG GCAGCACTTC TTGTGATTCA TCACTGTGTC 840
CTCTGTACCC GGCAACAACA CAGCATAGGG CCAGACACGT AGTGGTTGCC TTACTCATTT 900
ATTGAATGCT CTGCTAATTG TCAGGTGCGC TGCTAAAAAT TTTGGAGGCA TTAATTCACC 960
TTCTAAGGTT GGTACTATTA TCCCTTTTGT CTTTTTTTTT TTTTTTTTTT TTGAGACAGG 1020
ATCTCGCTCT GTCACCCAGG TGGGATTGCC GTGGCACGAT GACAGCTCAC TGAAGCCTAG 1080
ACCTTCTAGG CTCAAGTGAT CCTCCCACCT CACCCTCTCA GAGTGTTGGG ATTACTGGCA 1140
TGAGCCACTG TGCCCAGCTG TTATCCCTTT TCACAGATGA AGAGACTGAG GCTCAGAAAG 1200
ATGGAATAAC TTGCTCAGTT ACACATAGCT AGGAAGTAGG GAGCTGGAAT TTTGTGTATT 1260
TTTTTTTGTT TGTTTGTTTG AGATGGAATC GCTCTCTGTT GCCAGGCTGG AGTGCAGTGG 1320
CGCCATCTTG GCTCACTGCG ATCTCTGCCT CCCGGATTCA AGCGATTCTC CTGCCTCAAC 1380
CTCCTGAGTA GCTGGGACTA CAGTTGTGCG CCACCACACC CAGCTAATTT TTGTATTTTT 1440
AGTAGAGACG AAGTTTCACC ATGTTGGCCA GGATGGTTTT GACCTCTTAA CCTCGTGATT 1500
CACCCACCTC GGCCTCCCAA AGTGCTGGGA TTACAGGCGT GAGCCACGAT GCCCAGCCCT 1560
GGAATTATAC ATTAATGTAG GTTATCTTAA TCCAGAGCCA GCACTCATGA TCCCTGAACA 1620
AATGAACAAC TGCGGGTATG TGGTAAAATG AGCATTGAAT TTAGAGTCAG ACTTAAATTC 1680
AGTTAAGTAT TAGCTCTTAC CACTTTTCAA ATCTGTGACC CTAGGTAAGC CTCAGTTTTG 1740
TTCTGTTTTT TGGGGTTCTT TTTTTTGAGA CAGAGTCTTG CTCTTGTCAC CCAGGCCACA 1800
GTGCAGTGGT ACAATCTCGG CTCACTGCAA CCTCTGCCTC CCGGGTTCAA GCAATTCTCC 1860
TGCCTCAGCC TTGCCTCCCA GGTTCAAGCA ATTTTCCTGC CTCAGCCTCC CGAGTAGTTG 1920
GGATTACAGG TGTGTGCCAC CATGCCTGGC TTTTTTTTTT TTCGTCTTTT TGGTACAGAT 1980
GGGGTTTTGC CATGTTGACC AGGCTGGTCT CAAACTCCTG GCCTCAAGTG ATCTGCCCAT 2040
CTCGGCCTCC AGAAGTACTG GGATTACAGG TGTGAGCCAC ACACCCAGCC AGTTATTTTC 2100
TCATTCGTAA AATGAGAATA ACAGCCTCAA CCTGATCCAC CTCACAGTTG TGGCAGTGAT 2160
TGAGTAGAAT GGCAGAGGTG GACCAGTGAG GTTAGCTGAT GTGTGGCCCT GAACTCTGGA 2220
AACTGCTTCT CAGTGTGCAG GATTCCTTTT GTTCCAGCCT TACCTTCCTG ATGACCCTAG 2280
CCTTTTTCCA 2290