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

TagContent
EnhancerAtlas ID
HS091-10796 
Organism
Homo sapiens 
Tissue/cell
HepG2 
Coordinate
chr12:109990080-109991520 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs7974321chr12109990369hg19
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
INSM1MA0155.1chr12:109990743-109990755TGCCAGGGGGCA+6.62
IRF1MA0050.2chr12:109990318-109990339ATTCACTCTCACTTTCACTTT+7.67
Nr5a2MA0505.1chr12:109990897-109990912GCTGGCCTTGAACCT-7.25
PRDM1MA0508.2chr12:109990326-109990336TCACTTTCAC+6.02
Number of super-enhancer constituents: 1             
IDCoordinateTissue/cell
SE_05404chr12:109990807-109992123Brain_Cingulate_Gyrus
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr12109990893109991174
Number: 1             
IDChromosomeStartEnd
GH12I109553chr12109990808109992923
Enhancer Sequence
TAGCATGGGC CTGTAATCCC AGCTACTCAG GAGGCTGAGG CAGGAGAATC GCTTGAACCC 60
GGGAGGTGGA GGTTGCAGTG AGCTGAGATC ATGCCATTGC ACTCCAGCCT GGGTGACAGG 120
GTGAGACTCC ATCTCAAAAA AAAAAAAAAA ATAGTTCTCC TCTCCAGGCC TCAGTTTCCT 180
CATTTATAAA ATGGGAGCAA TGATGTCTGA GACCGTGTTC AGCTCTCATT GTCCTGCAAT 240
TCACTCTCAC TTTCACTTTG GCCCTGTGTT CCTGGAGCCA CATCCCCATC TTCTCATCTG 300
ATTGTGCCTG GCCACCTCTG GAGGCCACCT GTCTCCCCCA CCCACTCAGC AAGCCTGAGG 360
GGCCAGAGGT GCTGCCATGC TGTCCTCAGC GTCACCTGGG GATGAGCTTT TAGAACGTGC 420
TTTGAAAAGG GTCAAATATG ATTGAACAAC AATAGCTATT TTTTGGAGCT GCTATCATGT 480
CTGGGGCCTG TGGACTTATT TCTGAACTCT TGGAAATTGG TATTATTATC CTATTATAAA 540
AGATAAAGAG GCTTTGAGTG GTTAAACCAT TTGCTTAAGG AGATGCTGGA AGTGACAAAG 600
ATGGAATCTG AATTCAAATA GTAGTAGTAA TAGCAAACAA CTGTAATAAC AGGAGCTAAT 660
ATTTGCCAGG GGGCAATATT ACTCTTTTAA GTATTACCTC ATTAAACAAT CCCAGTGACC 720
CATGGGGTGG ATGTTATGAT TCCCATTCTA TAGGTGGAGG AGCAAGACCG AGACAGATGG 780
AATGACTTGC CCAGTCACCA AGGCAGGAGG TGACAAAGCT GGCCTTGAAC CTGAGCCTGC 840
CTGGGGCCAG TGCCCAAGCC AGCTGTTTGA CAGTCCTTCC CTGCACCCCA CAACCCTACA 900
AGCATCAAAG GTCACCCAGC AGCCTCTCCC AGCCAGCCCC AAGTGCATCT TCTCACCCTT 960
CCAGGCTGGA GCTATCTGAC CCTGAAACAG GCTGCTGAAG GCAGCCTTGG GAATCCTGAC 1020
TTAGCTCCCG AAGAGGGTCG CATGGGTTCT CTTAGAAAAG GGATTCTTAC CGGGAGGTTC 1080
CATGGACTTC CTATGACTGG ATGCAAACTT GTGAATATGT GTGTGTGCAT TCCAAAGGTG 1140
ACAAACCACA GCTTGAGAAG TTTCTGATTC TGTGGAATGG GAGAACACGA GGGATGTCCC 1200
CAAAGTTTCT AGGTCTCCGC AATCTGCCTG TCCCTGCCTC TGTTGGACTT TAGCACTATC 1260
TTCCAGGAGG ACTCTGAGAG AAGAAAAGCA ATAGGCCAAG GCAAGTTAAA ACTGTGCCGC 1320
CTGCCTCTAG CTGGACTGAC TGCAAAGATG CATTTATTCC AGCTTGTGTC AGTATTGCCA 1380
GAAGATTCTC AGGCCCCGCC AGAGGGGAGG GATGAGCCAC AAATCCTTCC AGGCACTGAT 1440