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

TagContent
EnhancerAtlas ID
HS091-48735 
Organism
Homo sapiens 
Tissue/cell
HepG2 
Coordinate
chr9:131465220-131467000 
Target genes
SNPs
Number: 2             
IDChromosomePositionGenome Version
rs13283282chr9131465481hg19
rs13289095chr9131466489hg19
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
FOSL2MA0478.1chr9:131466178-131466189GGGTGACTCAG+6.02
JUNBMA0490.1chr9:131466178-131466189GGGTGACTCAG+6.02
ZIC1MA0696.1chr9:131465622-131465636CGCAGCGGGGGGCG-6.44
ZIC3MA0697.1chr9:131465621-131465636GCGCAGCGGGGGGCG-6.97
ZIC4MA0751.1chr9:131465621-131465636GCGCAGCGGGGGGCG-6.4
ZNF143MA0088.2chr9:131466440-131466456CGGGGCATCATGGGTT-6
ZNF263MA0528.1chr9:131466077-131466098CCCCTCCCACCCCCTTCCTCT-6.03
Number of super-enhancer constituents: 2             
IDCoordinateTissue/cell
SE_34611chr9:131463389-131466894HCT-116
SE_34897chr9:131463390-131467108HeLa
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr9131466200131466876
Enhancer Sequence
GAACGGCGTG GGAGGGGCGC GCGGGCCCGG GGGGTGCGAG AAAGCCTCTG TCATCGCCCC 60
GGAGCCCCGA ACCGCGGCCG CTTCCCCCGA TCCTCCCCTC ACCCGCGCCC CTTCCCTGCC 120
CCTGCCCTGG CCCCGGCCCC GCGACGCCCT CGCAGAGCAG ACCTGATCTC CGGGTTCGGT 180
GGTTCCTGGA CCTTGCACAG TCTCCAAATC AGTCCGCGGC TGACCCGGAG ACTGAACCCC 240
AACCAGCCCG TGAGCGAGGA CGGCTGAGTC CGCAGTGTGC GCCACCAGGG TGGTCCCCAG 300
AGTGTCCTTA AGTCGGTTCT CCTCGGTGGG GCTCCAAGGC CGACGGGAAT TAGCCGGGAT 360
AGAAAGGCGG GGCACAGGGG CCTGGGGGGG TTAGAATGTG CGCGCAGCGG GGGGCGCAGT 420
CTGTGCGCGC TTGGCAGTGG CAGGAGTCCT TCCCGGAGCA CAGGAGGCAC GAGGGGAGCG 480
TAGATGAGAG GGGAGCGGCC TCCCCCGCCC CAGGGCGGGA ACCTTTGGGT ACATAGCGGG 540
TTCTAGAATG CGGAGGGGGC TGGGTTTCCT GCCAGAGCTG GCAGTAGGTG CGCGTGGGCC 600
CGGAGGACCG AGGCCATGTC TATCTGCTCC TGAGGAGGGA GAGGTGGTGT CCTGTTCCGG 660
AGCGAGTGGT TGGGAGGGGG GCATTTGCGG ACAGGAGTGG GTCCCCGCAA AGAGCGGAAA 720
GGAGGTGGTG TGTGTGTCCA TGTTGGAGTT CCAACCCAGG GCAGACGGGA CCATGGGGGT 780
GTTGCGGGGT GCGTGTAGAC TCCTTGAGCG CCCAAGCCAG TCGTTTAGGC CGCCTTCAGG 840
GCTGGGGCTC GGTCTGCCCC CTCCCACCCC CTTCCTCTGG AGGTCCCTCC GCCTGTTCCA 900
GACGTAGCTT GTACACATTT TCCGATTTCC TGCGGGGCTC CGCCCTGCAG CGGCAGCTGG 960
GTGACTCAGG ACCCCGGTGG CCGGGCCCCC AGCTCCATGG GACCTTTGTT TGCTCCGGTC 1020
TTTGGCTCTG GCCCTGTGGC CTAGGGCGGT CAGAGGATTT CCTGAGCCTC GCCCTTGCCC 1080
TCTGACAGCT GGGCCAGCAG GCCCCGCTGA GGTCTGGGGT GGGGGGGTCC CTGAGTCTGG 1140
GGTTGCGGCC CCTTCCACTG GGCTCAGGAG AAGATGGAAC ACAGAGAGGT AAGATGGGGT 1200
TCCTGCAACA GCCCGTGTTG CGGGGCATCA TGGGTTACCC GGCCTGAGGT CACCTTTGGC 1260
ACCGGTTGGT TTGAAATGCT GGCGGCTGGA AAGGAGGTGT TCCTGTTCCT GGCTCCAACC 1320
TGGGTGAAGC CGTGAGAGAG CCTTCTACTT CCTCCCGGGA GCTGAGCAGG GAGTGGGCAC 1380
CCGGAGACCT CCCCAGTTCC TCTCTGTGCC TCTGCTTTGC TACCTGTGGC ATTGGGACAT 1440
CAGGGGAACA AGCCCTGGCT CCCAGGCCCC TGGCTGCCTT CTCATGTGGC TTCGTGTGAA 1500
CCCCTATTCG GCGTAGCTTT TGTGGCTCCT GGACTCTACT TTGGGTCCCA GATGTAGAGA 1560
GAGCAGCCTG ATTACCCAGG GCTGCCAGGG ACAGCTGGGG CCCGAGAGAT GGTGGCCCCT 1620
CCTCTGTGTC TTGACTGTGG GCAAGTTACT TCACCTCTCT GGGCCTCAGT TTCCTCACTA 1680
GAAAATAGGG GTAATAGTAC AGGCGTGGTG GCTCACACCT GTAATCCCAG CACTTTGGGA 1740
GGCCAAGGCA GGTGGATCAC CTGAGGTCAG GATTCAAGAC 1780