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

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EnhancerAtlas ID
HS050-13134 
Organism
Homo sapiens 
Tissue/cell
Fetal_stomach 
Coordinate
chr11:76504250-76505510 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs10899282chr1176504698hg19
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ZNF263MA0528.1chr11:76505039-76505060TCCTCCCCCTCTCTCACCTCC-6.92
ZNF263MA0528.1chr11:76505042-76505063TCCCCCTCTCTCACCTCCTTC-7.26
Number of super-enhancer constituents: 3             
IDCoordinateTissue/cell
SE_00254chr11:76503160-76520678Adipose_Nuclei
SE_26826chr11:76503864-76505597Esophagus
SE_57060chr11:76503862-76504558VACO_400
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr117650426476505355
Number: 1             
IDChromosomeStartEnd
GH11I076793chr117650406076505493
Enhancer Sequence
CAGATGCCTC TTTACATCGG CTGTTACTAC CATTGCCTCA GTTCTGTATC TTCTGGCTGC 60
TGGGTGATGA CTGCCCTGTG CCTGTGCACA GCCCTTCACA GTTGGCAGTA AGGGTTAATC 120
AACTTAGGTG AAGAGGGCAG GGCAGAAATT GCCACCCTGT AGTGCAGAGG ACAAGGCTGA 180
GGCTTAAAGA GGGGCAGCGA GAGGTCCCCT CTGGCGGGAT AGCATTTGGG TCGTATTTTG 240
AGCTGCTGGT TACATAAGTG GGAGCTCATA TGAGGCCATT TGGCATTTCA CGGACCCCTT 300
GTATAATCAC CTCTGGGAAT CAAAGGGTAA TCTCAGGGCC TTTGTGCTGT TTGTTTAAAC 360
CCCAGGAAGG GTGGGTATGA ATGAGCAGAT CAGCTTAGCA GGGGAGGTGG GGCCTTTGGT 420
GGTAATGAGC CCTGCGGTGA GGAGCTCGCC CAGGGGAACA AAAGGGGCCT GAAGCAACTT 480
AATATTTTCC TTTTGGTTCC AGACATTGGA ACACTCTGTC CTGCCTCAGC TGGGACCATG 540
CCCAGGATGC ACCTGGGCTG GATTTAATCC TGAAATTGGC CTCTACAAAA GAAAGGGGTG 600
GGAGAGGAGG GTCCCACATG GGGAGGGGGG CAGGGGAGAA GAGTCCCACT TTTCCCTGCC 660
CCTGGGCAAA GCCAGAGTGC AGATCAAGTG GCTAGCCCTT TAAAGTTTCA TGCAGGGCTG 720
GTAATGCAAT CCTGCTGCTC CCTCCCACCC ACCTTCCAGT CTGGAAGGTG GGCAGGTCCC 780
TGGCCCATCT CCTCCCCCTC TCTCACCTCC TTCCTGAAGT CCAGAGGGAG GGATGGGCAG 840
GAGGGCAGGG GCCCAGAGCA GGGCCACCCA GATGAAGAGC CTGGCTAGAA GGAAGCTTAG 900
TGCCTTCTGT CTCCCAGGCT GCTGAGGGGC CACTGTGCAG GGCCGGGGTG ACGACAGACT 960
ATCCAATTGG TCTAGTTAGA AGCTCCCACT GCCCAACCCT CTCCTTCTCA TGCTGGCACC 1020
ACTGAGCACC ACCATCCCAG GAGCTACAGT GGACGTGAAC ACAGGCTTTG AATCCAACAG 1080
CAGTGGGTGG TGTGACCATT AGATGTGACA ACACGTATGT AGCACCTGGC ATCTGTAGCA 1140
GCCACCACTG TAATTGTACA GAGGGAACTG AGATCTGAGG AGGGACACTG GCTCATGCCA 1200
CAGCATGTGT CAGTGGGAAA AGCCCCTCCT GCACCCTGCC TCTCCACCAG CTACTCTGCC 1260