Tag | Content |
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EnhancerAtlas ID | HS048-26385 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr3:139238150-139239680 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr3:139239092-139239111 | TACTGCCCCCTGCTGTTGG | - | 6.18 | ZNF263 | MA0528.1 | chr3:139238348-139238369 | TGAGGAGGAAGGCGAGGAAAA | + | 6.82 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr3 | 139239222 | 139239506 | chr3 | 139238869 | 139239185 |
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| Number: 1 | ID | Chromosome | Start | End |
GH03I139519 | chr3 | 139238368 | 139239675 |
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Enhancer Sequence | AGAGGCTGTG GGAGCCCAGG TGAGAGTCCA GGGAGTGGGA TTCACTAGGG CTGGGCTCTA 60 AGGAGAGAAG AATGGAGCTG AAGGAGAGGA AAGGAGGCGC TGTGGAGAAG AGCTCCCAGT 120 AGCCCACCAC CCGGTGAAGG CCTGAGGTGG GACAGCGGGA AGTACACTTA GGAGCTCATC 180 AGGAGGGCAC CAGGGAACTG AGGAGGAAGG CGAGGAAAAT CCCACAGCCC AGCCTGGGCT 240 TGGCAGAGCA CAGATGAGCA CTGTGACACC CTCTACACCC CACATTTGAG CCCCCACATC 300 TTCCCTGAGC ACTGTGAGCC CTGCCATGTG CTGGGCATGC TGAAGGGAAG ACAGGCAGGA 360 GGAGGAGGCC CAGCCTGTGT CCTGGGGAGA TTTCAGTCTT AGTGGAGCAG AAAAGGCCCA 420 CCTAGCAACA CGGGGCTGAA AAAAGTGTTG GACTTCAGAG GCAAGGTGGT CCTGTCATCC 480 CAGCATAGCC ATGAGTGTGC CCTAGACTGG GACACATGTC GCAGATGTGG GCACACAGAA 540 AGTGCAGTGG GCATCACTCA TATTTGGGGC TGCCCACCTT CTTTTGAATA GCCGTCCCAT 600 ATGGGGCAGT TCTGTGTTAT GAGCCTGGCC TCCCCACAGT AGTGCTCAGC ACTCTGTTTG 660 CCCCTTGCTC ACTGTGTGGC TCTCAGCAAA TCCTTCCCTT TTCAGGGCCC CTGTGCTCTC 720 ATCTGTCACA TGGGGACATT AACTCAGGCC TTGAATGTAG AGAGCTAAGG TTCTAGGATC 780 CTTGTGTTCC TTGCCATGCT CAGCTGAGTC AGGACAGTCA GCAACAGCCG AATAAAGGAT 840 TTGGGAGAGG AGACTTATGG GAGATGGGTG TGGCGTTAGT GGGGCCACTC CCTGCAGGAG 900 GACCTCCCCA CCCCAGGCCT CCCACCTGGG CCTGCTGATC ACTACTGCCC CCTGCTGTTG 960 GGGTGAAGCC TGCAATGCGA CACATGCACG AGGGAGGCAG GTGGAGCCAC ATGTGCTCCC 1020 CCAGCTTTGC ATAGGAGTAA GTCTGCTCTC TGCTCCAGAG AGAAATGGGG CATAAAAGGA 1080 CTTGGGGGGC AGATCCTCTC TCTGATCCAG AAATTCACTC AGGGCACAGT CTAGTCCCAG 1140 GCTAGAGAGA ACGCAAAACA TAGTGTGGTT AATGTGTGGT GAGACATGTC ATGGGTAAAG 1200 ACTACTCATG ACCTCATGCC ATAAATAAGA CAGGACACCC ATTCACTTAT CCGTGCTCCT 1260 TCCATCCCAG GCCTGTAGAG GGAAGTGGGG ACCCAGAAAT CAGTCCTCAG CTTCAAGAAG 1320 CTCATAAGAA CACTTGGTTT CCTCATCAAC TGATCTTCTC TTCATGTGTT TATCCAGAAG 1380 GCTACTGTGC ATATGAAGGG TTCCGGATTC ACTCAGAGGC ACAAGAGACA ATTGCTTGTT 1440 TTCAGCTATG ACATACATTT TTGCCTCTTC TGGAAATATT AGTCAGGAAG TATAGTCATA 1500 GTCTTTGTAT TGGAAAATTA AAAAAAAAAA 1530
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