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

TagContent
EnhancerAtlas ID
HS091-10051 
Organism
Homo sapiens 
Tissue/cell
HepG2 
Coordinate
chr12:56394280-56395990 
Target genes
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs773125chr1256394954hg19
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
HEY2MA0649.1chr12:56395050-56395060GGCACGTGTC-6.02
MEF2AMA0052.3chr12:56394741-56394753TCTATTTTTAGT-6.27
MEF2BMA0660.1chr12:56394741-56394753TCTATTTTTAGT-6.32
MEF2CMA0497.1chr12:56394740-56394755TTCTATTTTTAGTAG-6.57
Npas2MA0626.1chr12:56395050-56395060GGCACGTGTC+6.02
SOX10MA0442.2chr12:56394562-56394573TTCTTTGTTTT-6.62
Number of super-enhancer constituents: 2             
IDCoordinateTissue/cell
SE_28263chr12:56394730-56396550Fetal_Intestine
SE_28988chr12:56394361-56396611Fetal_Intestine_Large
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr125639533356395857
Number: 1             
IDChromosomeStartEnd
GH12I056000chr125639456656396278
Enhancer Sequence
CTCAGCCCCG GTTCCCGCTC GCACCTCTCC CTCCACACCT CCCTGCAAGC TGAGGGAGCC 60
GACTCTGGCC TTGGCCAGCC CAGAAAGGGG CTCCCACAGT GCAGCGGCGA GCTGAAGGGC 120
TCCTCAAGTG CCGCCAAAGT GGGAGCCCAG GCAGAGGAGG CACCGAGAGT GAGCAAGGGC 180
TGTGAGGACT GCCAGCACAA TGTCACTTCT CACTAGGATT ATAAGGGTGA GCCACCACAC 240
CCAGCTCTTT TATTACAGTA TAATGTTATA ATTTTTTTCT TTTTCTTTGT TTTTTTTTTG 300
AGACGTTTGA GACGGAGTCT CACTCTGTCG CCCAGGCTGG AGTGCAGTGG CGCGATCTCG 360
GCTCACTGCA ACCTCCGCCT CCTGGGTTCA CGCCATTCTC CTGTCTCCGG AGTAGCAGGG 420
ACTACAGGCG CCCGCCGCCA AGCCCGGCTA ATTTTTTTTT TTCTATTTTT AGTAGAGATG 480
AGGTTTCGCC GCGTTAGCCA GGATGGTTTC GATCTCCTGA CATCGTGATC TGCCCGTCTC 540
AGCCTCCCAA AGTGCTGGGA TTACAGGCGT AAGCCACTGC GCCGGGCTAA TTTTTCTATT 600
TTGTTATTGT TGTTAATCTC TCTTTTTTTT TTTTTTTTTT TTTTTTGAGA TGGAGTCTCT 660
CTCTGTTGCC CAGACTGGAG AGCAGTGGCG TGATCTCAGC TCACTGCAAC CTCCACCTCC 720
CAGGTTCAGG TGATTCTCCT GCCTCAGCCT CCCGAGTAGC TGGGGTTACA GGCACGTGTC 780
ACCATGCCTG GCTTATTTTT GAATTTTTGT AGAGACAGGT TTTCCCCATT TTGGCCAGGC 840
TGGTCTCAAA CTCCTGACCT CAGGTGATTT GCCCGCCTCA GCCTCCCAAA GTGCTGGGAT 900
TACAGACGTG AGCCACTGCG CCGGGCATTG TTGTTAATCT CTTACTGTGG GTAATTTAGT 960
AATTAAACTA TAAGAGGTAT GTATGTATGG GGGAAAAAAC AGTAATATAG GGTTTGGTGC 1020
AATCTGTGGT TTCAAACATC TACTGGGGGT CGTAGAACAT ATCCCCAGTG GATAAGGGGG 1080
TACTACTGTA CTTGTTGGCT CTTCATGTTA GCTCTGCTAG GCAGATGTCA TTTCAGAGAT 1140
GAGGAAGCAA GTTCAGAACG GCTTGGAATC TTGCTCAGGA AATCGGGCTG GTTAATGAAT 1200
AACAAGAGAT CCAGTTTCAC AAACCCAAGG CATTTTGCCC CCAGAATCTG GGCTTCTTCA 1260
CCCATTTAGG CTGTCACTAC TTTTTTTTCA CTTTTTTATC CCTGTTTAAG TCAGTCTGAC 1320
CCACAGTTGT CCTCTGCTGA CTTCAGAAAT AATAATCTGG CCAGTAGACA TTTGGTTTCG 1380
GTCCTTTAGG CCCTTCGCCC CAGGCATCGT TCTCTATGGT GGACAAAGTT CAGAATGGAA 1440
GATGGGAGAA AGGTGATTCT GATTCTAGAA GCACCCATCC CTCCTACCCC ATTCCCCACC 1500
CGCATTACCT GCCATCCTGT CAGCACAGTC TGTCTCTGAA GTGCTCCAAG TTTTCTCTAA 1560
GGGCCCATTT GGACTCCCAC TCTCAAGACT CCTCACTTGC CCAGAAAGCT CCTTGCTGAC 1620
CTTCTCTGTG TCTTCCTCTC ACCCATTCCC TTAGGCCTCC CTAATATCCC CTCCCAGGGT 1680
CTCCCTATCT TGATCCCAGA ATCTTCCTTC 1710