Tag | Content |
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EnhancerAtlas ID | HS050-03900 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr1:119589160-119590180 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr1:119589931-119589949 | GGAAGAAAGGAATGAAAA | + | 6.4 | Nr2f6(var.2) | MA0728.1 | chr1:119589199-119589214 | TGAACTCCTGACCTC | - | 6.22 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I119046 | chr1 | 119589038 | 119590495 |
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Enhancer Sequence | AGGAAAGACA GGGTTTCACC ATCTTGACCA GACTTGTCTT GAACTCCTGA CCTCGTGATC 60 CACCCACCCC AGCGTCCCAA AGTGCTGGAG TTACAGGCGT GAGCCACTGC GCCCAGCCCC 120 AAATTTGTTT GTTTCAACCA AATTTAATCA AGCTACCAAA CCTGATGACC TAGAATTTAA 180 GGCCTATGCA TCCCGTTTCT TTACTCTGGG GATTACAAGC CCTTCATCAA CTGTGGCTTT 240 TTTTTTTTTT TTCATCCACA TGATTTCCTT AAAAAGCAGA GACTGCTGCC AACTCTGAAA 300 AGTGGCCCCA AATGTGTTCT TTGTGGGTTT TGCAAAAAGA ACATAAAGGA GTGGAGCTGA 360 ATCAGCCCAG GCCTGTTCTA CTAACAAGGA ATCGCCATCT GTTGTAAGAT AGTTTCTCAT 420 TTTTTTCCTC AAGTTATAGA GAGGGAAGAG TTGTTTTTCA CGTGTTTGAT AAGGAATCAC 480 TTTTAAAGTT TTGCAAGTCC CTGGGCTGAA TCTGTCATCT TTCTTCCAAG AGGCATTTGG 540 GTTTCATTCA GGGCAGTGAC ATTGACACAC TGTCCATGCA AATTGCTAAC TGCTGCTGTA 600 AACAAATAGC TATCAGACAA AAACAGAAAC TAACCCTGGA TGTAGGCAAG AGGACTAGAG 660 TTGCTTCCAA TCACCAAGGA AAATACATTC CCATTAGAAG TAATAAAACA AGAGCTGTTT 720 TTCTGGCATG AAGAAGTAGG AGAGAATTTT TTTTTTCTTC TTTACTGAAT TGGAAGAAAG 780 GAATGAAAAC ACAGATAATA ACCATGGATA TGTGGAAGGA GACAAGATGA CGCCTCTTTA 840 ACTCTGATTC AAATGCTTAG CTTTGGTGAT ACGCAAAAAG CTACCACTAT GTCTCCACGA 900 AGCTGAGTAT TTTCCTTGGA GTAGCTTTTT ATTTGGACAT ATGGAATGAA ACTTACTTAA 960 TATTCTGCAG AGATCTTCCT GGTGTTTCCA AAATGGTGAG CATAAAATTA ATTCAAATTA 1020
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