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

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EnhancerAtlas ID
HS050-54481 
Organism
Homo sapiens 
Tissue/cell
Fetal_stomach 
Coordinate
chr5:74935870-74936980 
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
GATA2MA0036.3chr5:74936198-74936209TTCTTATCTGT+6.14
Gata1MA0035.3chr5:74936198-74936209TTCTTATCTGT+6.62
HNF1AMA0046.2chr5:74936663-74936678AATTAATGATTTACC+6.68
HNF1BMA0153.2chr5:74936664-74936677ATTAATGATTTAC-6.67
NKX2-5MA0063.2chr5:74936887-74936897CTCAAGTGGT-6.02
SOX10MA0442.2chr5:74936645-74936656TGCTTTGTTTT-6.02
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr57493589374936028
Number: 1             
IDChromosomeStartEnd
GH05I075639chr57493566174937528
Enhancer Sequence
TTTTTTTTTT TGTTTTGAGA TGAGGTCTCA CTCTGTTGTC TAGGCTGGAG TGTGGTGATG 60
CAATCCTATC TCACTGTAGC CACAACATCC TGGGCTCAGG TGATCCTCTC ACCTCAGCCT 120
CCTGAGTAGC TGGGACTATA GGCATCCACC ACCATACTCG GTTAATTTTT TAAACTTTTT 180
GTAGAGATGG GGCTTTGCCA CGTTGCCCAG GCTGGTCTTG AACTCCTGAG CTCAAGTATT 240
CTGCCTGCCT CAGCCTCCCA AAGTGCTGGG ATTACAGGCC GAGCCACTGA ACCCAGCCAC 300
TTTGACACTT TTCAGCTGAG GTTTAGTTTT CTTATCTGTA ACATGTGGAT AATATTAACC 360
CTGCCCTTAT AGCATTGTGT GATTTAACTG TGCCAAAGCA TATAGTCTTG GCAGTACAAG 420
TTGACACATA GTTGTTCAAT AAATGCCATC CATTATTAAG AGTAATGCAC AAAAGGCATA 480
GAGAAAGCAT GTTGTTTGTC AAGTAATTTC ATTCCATGAC AAAGGGCAAT TAAATTTAAC 540
TTATTTTTCC TTTTGTTGGA ATGGAGAAAC ACCATTCTTT CTGAGTGTTG AAGGAGGTCA 600
TGAAGAGTGC AGCAAAGTGC TGCTGACAGC AGGAAGTGAC ACCAACATTC CAAATAAAGT 660
ATGTGTTCCA GACCATGTTC ACTCATGCAG TGGGAAGGAG ACTTAAAATG TTCTTTGGAA 720
ACACTGGTCC TACATTGATC CACTCACTGG TACTTTAGAA TTAATATTTA TAATATGCTT 780
TGTTTTTGGT AAGAATTAAT GATTTACCTC TAATATTCCC CAGTTACTGT GTCCTCAAAA 840
GCAATGCCAT TCTTTCTATT CTTTTGGGGA AGGAATAATT GAAAATGGGG CAAAATGAGC 900
AAGTACTTGT CACTTCTTAG AAACAGACAC TCTATTCTAC TTTGTTTTTT CATAGCAACT 960
AGTGCACGCT TGGCTTATAC AGAGAAGACG CTGAAAAAAA AGTTTATTGT GTGAAAGCTC 1020
AAGTGGTCAG CCTGGTGCAG GAAGAAGGAA GGATGGTGCC TTCCTCTAAA TGCAGAATAC 1080
TTTTGTATGT AGTCATTGTG CTAAGAACCT 1110