| Tag | Content |
|---|
EnhancerAtlas ID | HS180-40634 | Organism | Homo sapiens | Tissue/cell | Small_intestine | Coordinate | chr5:176119320-176120850 | 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 | CTCATTCTGT TTGCATTTAC ATCTCATTGC GTGAGAGAGA CAATGAGCCC ACAAACAGGA 60
AGCCATCTGA GAGTGGACAA GGCTTCCTAA AAGTCTTAGG AAGAAAAAAA GGGAGGTGAT 120
GTGATAGAGA CTGGTGTGCA CATGGCACGG AGTCTCTGTG ACTGGGCTGT GAGGAGGTGG 180
CGCTGGAGCT GAGACCTGAG TGTGAAGAGG ACAGGGATTG TGGGGAGGAA GGCCAGGGGG 240
CCGGAGGGCA ATGAGTGAGG GTGGAGGTGA GACCAGCAAG TTGGGCAGGG CCAGGTGACA 300
TGTCTTGGTA AGCACAGTGA CATGTTTTGC ATTATTCTAA ATGCAAAAGG GAAGCCACTG 360
GGGGCTTTCA GAAGGATATG GGACAAAGAT TTGAGTATTA GGCACGCCCC AGGTGCTTAA 420
TAAATGTCTG CAGCCTGGGG TAGGGCGTAT CCAGCCGGCC CTTCTCAGGC TCAGCTAGTC 480
CCTCTCTTGT CCTGCCTACC TCACACCCCC AGCTCCTGAG CAGGGGACCC CTCGGGCTGC 540
CTTTTCCATC TTCTTGGCCC TGCCTCATCC TCCCCTAGGG CTGTTTGCTC CCTCCAGAGC 600
AGGCGACCAT AATTGCTGCT TTCCACAATG ACATAAAAAT CTAAGAGGCA CAATCAATAC 660
AGCGCACACA CATCATCGTC TTTCATTGCA AACGATAAAA GTGTAAACAG CAGGGGTGGC 720
GGCAGCTCTG GAGGCTGCAG TGGGGGCAGG GCGGGCTGCC ACCACTTCCC TGACTGTCAC 780
CCTTCTTCTG GGACACAGGG CTCTTCCAGG TGCGAGCGGG AGTGCCTTCC CCACTCTGGG 840
GAGTGGCACC CCTCATTAAA GCCCATTCAG GGAAGTGGTT TTTCCTGTTT TTGCTTCCAG 900
ATGCAGCAAC CCCAGTTTCT TTAACCCGAC TTCAGAAATC CAATTTGTCC TCTGTACTTT 960
AAAAGCTTTT CCCTTGCTTC CCCTGCATCC AAAATACAGA GCTAGGGGTG GCTTCTGGTG 1020
GCAGAAGAAC TTGTTGGGGT TTTGCCTGTC ACAAGCCCAT GAACTGACCT CGACCCCATT 1080
TTAACCCCAG CTCTTGACAG CCAACTTCTT TCGCCACCTG TCCAGCCTGC CACCCACAGC 1140
TTTTCTTGGA ACGTGCACAG AAACCATTAT ATCCCCAGCT CCCACACACT CCCGGCGACG 1200
ACTTCCTCAA ACTAGTTACT TAATGAACGT CATCCAATTC CGATTCCGTC TTGCTGTAGT 1260
CTCATTTGCG AAAGCCAATC TGCTTTATGA TTCTAACCTC TGGCTAGCAA CTGCTCCCAA 1320
TTTCATGTCA TCCATAAACT TGATGAACGA TTAGCTTGCT TCTCTGCAGT CATTCATTTA 1380
TTTATTCAAC CGGTATTTAG TGAGCGCCTA CTGGATGCTG GGTGCTGGAT ACAGAGTTAC 1440
AGGAGACGCA GGTCCTGGGC TGAAGAGACT CCTGTGGGGA GGCGGAGCCC ACGTGAAAAT 1500
GGTTCCCATT TATGTGATCT GTGCTCAACT 1530
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