| Tag | Content |
|---|
EnhancerAtlas ID | HS040-29210 | Organism | Homo sapiens | Tissue/cell | Esophagus | Coordinate | chr5:176119400-176120790 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxo1 | MA0480.1 | chr5:176120021-176120032 | TGTAAACAGCA | - | 6.14 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH05I176692 | chr5 | 176119654 | 176120597 |
| Enhancer Sequence | GGCTTCCTAA AAGTCTTAGG AAGAAAAAAA GGGAGGTGAT GTGATAGAGA CTGGTGTGCA 60
CATGGCACGG AGTCTCTGTG ACTGGGCTGT GAGGAGGTGG CGCTGGAGCT GAGACCTGAG 120
TGTGAAGAGG ACAGGGATTG TGGGGAGGAA GGCCAGGGGG CCGGAGGGCA ATGAGTGAGG 180
GTGGAGGTGA GACCAGCAAG TTGGGCAGGG CCAGGTGACA TGTCTTGGTA AGCACAGTGA 240
CATGTTTTGC ATTATTCTAA ATGCAAAAGG GAAGCCACTG GGGGCTTTCA GAAGGATATG 300
GGACAAAGAT TTGAGTATTA GGCACGCCCC AGGTGCTTAA TAAATGTCTG CAGCCTGGGG 360
TAGGGCGTAT CCAGCCGGCC CTTCTCAGGC TCAGCTAGTC CCTCTCTTGT CCTGCCTACC 420
TCACACCCCC AGCTCCTGAG CAGGGGACCC CTCGGGCTGC CTTTTCCATC TTCTTGGCCC 480
TGCCTCATCC TCCCCTAGGG CTGTTTGCTC CCTCCAGAGC AGGCGACCAT AATTGCTGCT 540
TTCCACAATG ACATAAAAAT CTAAGAGGCA CAATCAATAC AGCGCACACA CATCATCGTC 600
TTTCATTGCA AACGATAAAA GTGTAAACAG CAGGGGTGGC GGCAGCTCTG GAGGCTGCAG 660
TGGGGGCAGG GCGGGCTGCC ACCACTTCCC TGACTGTCAC CCTTCTTCTG GGACACAGGG 720
CTCTTCCAGG TGCGAGCGGG AGTGCCTTCC CCACTCTGGG GAGTGGCACC CCTCATTAAA 780
GCCCATTCAG GGAAGTGGTT TTTCCTGTTT TTGCTTCCAG ATGCAGCAAC CCCAGTTTCT 840
TTAACCCGAC TTCAGAAATC CAATTTGTCC TCTGTACTTT AAAAGCTTTT CCCTTGCTTC 900
CCCTGCATCC AAAATACAGA GCTAGGGGTG GCTTCTGGTG GCAGAAGAAC TTGTTGGGGT 960
TTTGCCTGTC ACAAGCCCAT GAACTGACCT CGACCCCATT TTAACCCCAG CTCTTGACAG 1020
CCAACTTCTT TCGCCACCTG TCCAGCCTGC CACCCACAGC TTTTCTTGGA ACGTGCACAG 1080
AAACCATTAT ATCCCCAGCT CCCACACACT CCCGGCGACG ACTTCCTCAA ACTAGTTACT 1140
TAATGAACGT CATCCAATTC CGATTCCGTC TTGCTGTAGT CTCATTTGCG AAAGCCAATC 1200
TGCTTTATGA TTCTAACCTC TGGCTAGCAA CTGCTCCCAA TTTCATGTCA TCCATAAACT 1260
TGATGAACGA TTAGCTTGCT TCTCTGCAGT CATTCATTTA TTTATTCAAC CGGTATTTAG 1320
TGAGCGCCTA CTGGATGCTG GGTGCTGGAT ACAGAGTTAC AGGAGACGCA GGTCCTGGGC 1380
TGAAGAGACT 1390
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