| Tag | Content |
|---|
EnhancerAtlas ID | HS180-46023 | Organism | Homo sapiens | Tissue/cell | Small_intestine | Coordinate | chr7:138645320-138646560 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Hnf4a | MA0114.3 | chr7:138645990-138646006 | AAGGTCAAAGTACATA | + | 6.18 |
| | | 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 |
| GH07I138960 | chr7 | 138645646 | 138646560 |
| Enhancer Sequence | GCTGGGATTA CAGGCATGAG CCACTGTGAC CAGCCACAAA AATAAAAAAA TTTTAAATAC 60
ATGCTACAGT GTTTCCAACA CCAGCAAAGG GCTGAACCTC CCAGACACCC CAGGCTGGAG 120
CCCAGGCTGC CACGGCAGGC ACCTCACAGA AGCGTATCTG CGGCCAGAGA GTAAAACTGC 180
TCTCTCCATA TTGCACGTGC TTTTCTCAAG AAACGCTTTC TAATGCCCTG TAGGACTAGA 240
AACACAAGCG GTGGTGTCTT CCGGATTTTC CAAAGAGATC AAACTATTAT GAAGCAAAGT 300
CTCCAGGAAC ATAAATGATA AGAATGCTGG GAAATTCTAA AAGCACTGCA AACTCCACAC 360
AATAAGGGAC ATGAAAAGAG ATGAATGGGA CACTAAATGT GTCTTTCCCC CATGCCCTCA 420
TAACCTCTCC CTGTGCAGTT CTGACAGAAG GGCCCCTTGC AGGCCATCGG ACAGCACAGC 480
CAAGGAGCAG GAGCCATCTG TCCTGCACTT GGATCCGGGT GACGGCCAAT GCCCACAACC 540
TCTTGCCCAC CAAAGAGTGG GGTCTCCTCT AGGCACACAC TGGGAGGTTA AAACCCCATT 600
CTAAGTTGCT CCTGTTGTCC TCGGAGCAGT CTCAAGACTT GAAGTTTGGC ACTTGGAAGG 660
CACCCAATTA AAGGTCAAAG TACATAGGAG GGCTCCATGC CAGGAGATCT TGGCGTTCTT 720
CTTTTGAAGT CTATGACGGA AATGCTGCAT TTTGAAAGCT ACTGGGGGAA GCATTGTGAG 780
ACTGAGGCAA ACACAGCAGC TGGGCAGAAA ATAGATCTAT TAGGCTCCTA CCGTGGGCTG 840
AGAGAGCTGC TTTGGGATCG GCCCCATGAT GCGCTTTCCC TACCCTGCCA CGAGGCTATC 900
ACCCCCCACA GGGACCACGG GAGGCTGCTG CTGTACACAA AAGGTCCTCA CCTCCTCCAG 960
GCCTGGCCCA CTCAACAATC CTTTCACAGC TTCCTGCTCT ATTCCTTCTT CTGTGATCCA 1020
CAGATACTAT AATTATAAAC TACTTTTTTC ATGGAACCTG ACCTGCTCCT GCCCCATCTC 1080
ACTTAAGTGA TGATGATGCC ACTATCAAAA AGAAAAATGC GACCAGGCAC AGTGGCTCAT 1140
GCCTGTAGTC CCAGCACTTT GGGAGGCTGA GGCAGGAGAA CTGCTTGATC TCAGGGGTTC 1200
AAGGCTGCTG TGAGAGATGA TCATGCCATT GCACTCCAGC 1240
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