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

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EnhancerAtlas ID
HS116-22814 
Organism
Homo sapiens 
Tissue/cell
Left_ventricle 
Coordinate
chr22:50697030-50697840 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs742184chr2250697119hg19
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
MAFGMA0659.1chr22:50697222-50697243CAACTGCCGCCTCAGCATTTT-6.15
MITFMA0620.2chr22:50697209-50697227ACAGGTCATGTGACAACT+6.02
MITFMA0620.2chr22:50697209-50697227ACAGGTCATGTGACAACT-6.02
ZNF263MA0528.1chr22:50697644-50697665TGTGGAGGGAGGAGGAGAGGG+6.39
ZNF263MA0528.1chr22:50697648-50697669GAGGGAGGAGGAGAGGGAACA+6.61
ZNF263MA0528.1chr22:50697654-50697675GGAGGAGAGGGAACAGAGGGG+6.66
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr225069734450697750
Enhancer Sequence
GGGCTCCTGC CGCCTGACCC TTTCACCCCT CTTCACCCCA ACCAAACAGA TCCAGGCCCA 60
GGGTGGGGAC AGCGCTATGG AAAGAGGCCA GGCCTCTGCT GGTGAGGCCC AGGCGGACAG 120
CACCGTGACC CACCAGACCT GGTCCCCTCA GCACCCCTGG TTGGGGAGAT AGACAGTAGA 180
CAGGTCATGT GACAACTGCC GCCTCAGCAT TTTGGGGTGA CGGTCCCAGG GAGGCCTGGA 240
GTTTTGCACA GCCAAGGGTG GAGGGGCAGG TAGACATGTG GGCTGCGGGA CACCTGGCAG 300
AGGGCACACA CAGAGTGGCC GAGGCAGGAG GGAGCACACT TGGATAGTTT GAAGAATACA 360
GGGAGGGAGG CCAGGTGGCG GAGGCCCAGG CCAGGGAGGG GCTGAGGAGA GGCCAGAGGG 420
AGCCGGCAGG GCAGCACACA CCAGGTGGAA GTTTGGCTTT GATCCCAAGA GACGGGGACG 480
ATTTAAATGG GGACGTGAGG CTAAATGCGT CCTCCTGGCC GTGGTGTAGG AACCGGCCAG 540
AGTGAGGTAA GAATGGACAC AAGCTGGAAG GACAGCTCCG CCGGAGCCAC GTGGGCCAGA 600
GCCATGGGCA AGAATGTGGA GGGAGGAGGA GAGGGAACAG AGGGGGTGTC CAGGGGGCAG 660
CGGGGACTGT GGACATGAGA GCTGGAGGGT GCCCGGGAGA GTGCTTTAGC AGAAGACGGA 720
GAGCAGGGTC CTGTGGGCTA GGGGCCACAG GACTTGGCCT GGCCTCTGTG GTATGGGGGC 780
TGGCCTGGAG AGGGAGGCGG CCTGGCAGGA 810