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

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EnhancerAtlas ID
HS050-21097 
Organism
Homo sapiens 
Tissue/cell
Fetal_stomach 
Coordinate
chr14:75670200-75671410 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs7147775chr1475670211hg19
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Gata4MA0482.1chr14:75670740-75670751TCTTATCTCTT+6.02
IRF1MA0050.2chr14:75670359-75670380AAAAAAAAAAAGAAAGAAAGA-6.25
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr147567070675670802
Number: 1             
IDChromosomeStartEnd
GH14I075203chr147567020475671796
Enhancer Sequence
ATACAAAAAT TAGCTGGGCC TGGTAGCACG TGCCTGCAGT CCTAGCTACT TGGGAAGCTG 60
AGACAGGAGA ATCACTTGAA CCTGGGAGGT GGAAGTCACA GTGAGCTGAG ACCACGTCAT 120
TGCACTCCAG TCTGGGTGAC AAGAGCAAAA CTCCGTCTAA AAAAAAAAAA GAAAGAAAGA 180
GAGAGAGAGA GACAGAGACA GAGAGAGGCA GGAGATGTGT TAGAAAGCTA TTAGATGTCA 240
ACCATTGTGG AAGGAATGAA CCAGGCTGGG CTGGCGGAGA ATGGAACGAA GTAACCAGAT 300
ATGAGGCACA AGGGCTCAAA AAGTAGTTTG TAAACTCGAT TGAGCCATCT GGGGCAGTTG 360
GGACCCCAGG AGTTCATCTC CAGCCTACAC CAGAATCCTC TCTGGGAAGT GACTGGGAAT 420
CTACAATTTT AAAACACACA GCCATCCTCC ATAGAAGACA CTGGTCTGTG TAGATGGGCA 480
TTTGGAAACC ATTGATCTAT TAGACCGTTT TTTCTAAATG TCCTCTAGTC CAGTGTCTCA 540
TCTTATCTCT TTGCTCTTGC AGTTAAGCAT TATCAAAGCT TAGCTTTTGA GTACTTGCAA 600
TTTGTACTCA TTACATTTAG AGTCATATAT CTGCAAGATC TCTTCTGAGG TCTTTGGAAT 660
GAAAACAAGG ACAGAGAGGT ATGTTGGCTC CTAACCGTCG CCTTATTTTG TTAGTGTGTC 720
TGGGGCTTGT GGCTTTTGAC AGGGACTCGA GAGATGACTT TGTCAGCTTT TCCTTTCACT 780
ATAGTAAGTC TCCATAACAA ACACACCCAA GTCTGGTATT TCTGAACTTA TGGCTCTGTA 840
CTGAATACAT GCTGTTCCTG GAGCCAGGCT CATTTTGCAG TTTCTCCTCC CAACTCCACC 900
CTTTGGTCCT GCTGATGGGC TCATTCAGCC TTGGCATGTG ATAAACCTCA GGTTCTGGGA 960
GTTTTCTCTA GGACACTGAA GAACAGTATT GACTTTTCAG TAATTGCTGG AGTTTAAAAG 1020
GAATGGTGAT CTTTGGGAGT GGGAGTGTGG TACAGGTGGG CGAATAGGAC TTACGGTGCC 1080
AACTGGCTTC TCCCCATTCC TATAGTGAGG GGACTCATAA GAATGAATAA CTAGGAAAGG 1140
GTTTGCCAAA CTTCAGTTGT TTGAATACCA TCCTCATGAT TTTTGCCAAA TCTTCATGTT 1200
ATCCATCTGC 1210