Tag | Content |
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EnhancerAtlas ID | HS050-01261 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr1:25992790-25993750 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr1:25993600-25993618 | GGATGGGAGGGAGGTAGG | + | 6.13 | ZNF263 | MA0528.1 | chr1:25993586-25993607 | GGAGGAGGATGTGAGGATGGG | + | 6.02 |
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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 |
GH01I025666 | chr1 | 25992892 | 25993691 |
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Enhancer Sequence | CCAACCCCAT TTTTCACTTA GTGACTTCAC ATCCAGGAGG GGGGCTGTTG AATTCCAGCT 60 AATGAGCCTC ATCTTTTTAC TCCTCTTAAG TGGTCCCAGC TAGACCTGGA GTCAAATCTG 120 AGAGCAAACG GTAGCACACA TCTTTCTCAG GTTCACAAAC GGAACACCAA GTCCATAGTG 180 AAAGGGAGAG GAATTTCTTC CTCTTGCTTA GAAAGACAAA AAGAGCAGCT TCTCAGGGCA 240 GCAGGTTGAG TAGAAGCCAT CCTCCTTAGA AAAGGCAGAC TTGGTGTTTA ATTAACAGCA 300 GCTGGAAAGG ACCCCACTCC CCCCACCACT GGCAGCTGAG CCGACATCGT TTTATGTAAT 360 AGATTCTTTT CAGCTGCTGT GCTCAGAATT GAGAAAACCT GATGGTTTCC TCCTTTATAC 420 AAAACATACG GCTGTCAGCG ACAGAAATCT CAGCCAGGCC TTTCTTTTAT GGGGATATTC 480 TAAAAGGGCC TGTCTCTGAG ATTTTGAAAG AGTCCCGGTG AGCCACCATC ACCCATAGTT 540 GTGCCTCAAA AGCAAGTGCA GGGAAGAGGA ATTCTGTGAA GGTTTTGAAA CACCTGTCAT 600 GGGCCGTGGG TTCATTTGTG CCCTGCCTAT GGCAGGGTCT GTTTTGCCCA CTGGCAGGAG 660 GCTGCTGTTT CCTATAGCTG GTTTACAGGC CCCAGCAGGA AGTCCCAGTT CTGGAGGCAG 720 CATAGGAAAG AGAAAATCCT GGTCTCCTGT TAGAAGTCAG AGCAGCAGAC CTAGAGAAGG 780 TGTATTCAGT TCTTGGGGAG GAGGATGTGA GGATGGGAGG GAGGTAGGAG GAGAGAGCTC 840 AAAATCCCAC CAGTTGAAGG CCTGTGTGAG CTTTAATTTT GGCCATTTAA ACAATTCAAA 900 GAGGCTGGGA GTGGTGGCTC ACACCTGTAA TCCCAGCCCT TTGGGAGGCT GAGGCGGGCG 960
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