Tag | Content |
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EnhancerAtlas ID | HS048-27277 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr4:4576260-4577560 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
GFI1 | MA0038.2 | chr4:4576692-4576704 | TGCAGTGATTTT | - | 6.11 | RREB1 | MA0073.1 | chr4:4576611-4576631 | ACACAACACACACACACACA | + | 6.19 | ZNF263 | MA0528.1 | chr4:4576576-4576597 | CTCCTTCCTCCCCCTTCCTCC | - | 6.37 | ZNF263 | MA0528.1 | chr4:4576575-4576596 | CCTCCTTCCTCCCCCTTCCTC | - | 6.44 | ZNF263 | MA0528.1 | chr4:4576569-4576590 | TGCCCTCCTCCTTCCTCCCCC | - | 6.53 |
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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 |
GH04I004574 | chr4 | 4576041 | 4577727 |
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Enhancer Sequence | AAACTGTGAG TCAATTAAAC CTCTTTCCTT TATAAATTAC CCAGTCTCAG GTATGTTTTT 60 ATTAGCAGCG TGGGAATGGT CTAATACAGT ATCCAACCAA TCAAGTGCAG CTTCAGAGAC 120 CTTGGGCTTT AAGAAAAGGG CTGAAGGCCA GAGAAGATTT CTCAGTGAAG GTGAGTTGAG 180 CAGGGCCTTA GGGGAGGGTA GGTCATTAGG TAGAAAGTTG GGCATTGCAA GGCGAGAAAA 240 CAGTGTATGA GCTGCTGTGA AAGACATGGG AAGGGGAGAA GCTCAGGCTG TTTCTCCTCC 300 ACCAGAGAAT GCCCTCCTCC TTCCTCCCCC TTCCTCCCAA CACACACACA CACACAACAC 360 ACACACACAC ACACACACAC ACCAGTTTTC TCCCGGAAAC TGAGCTAATC CAGCCACGCC 420 CCGACAGACA TTTGCAGTGA TTTTACACAC ACACACACAC ACACACACAC ACACCAGTTT 480 TCTCCCTGAA ATTGAACTAA TTCAGCCAGG GCCCCCCTAC AAACGTTTGT AGTGATTTTA 540 CTCCCAGCGT GGACTCTCCT GCCCGGTCAG CTTCAAGGAT TCCTTTGGTC CCAGAAATAG 600 CCAAGGTGGC GGTGAAGGGA GGAGCTGTTT CATTTCCGAA ATGAAAAAGT TTAAGATAAT 660 TACACAGACG GCTTGAGCCT GCAATGGACA AAAAGTTTCA TTATTGGACC CCTTTGGGGA 720 AGGCGCCTCC CATCCCCAAA GGAGCGGGTT AACCGCTCGG CTGGCGCGGC CCCGCCCGGG 780 TCGCCGTCTG AGAGGGACGG TCGCGCCCCC TTTGAAGTGC GGCCGCGCCT AATGAGGGAC 840 TCGCTGGGCC TCGGGATCAA GTGTCAGCGC CGCCCCAGAC GCCGCAGGGC AGACAAAGGG 900 CGCGGGCCGC CTGGCGGCGC TGGGAGGAGC GTGCGGCCCG CGGCGCTGAG CGGGACAAAG 960 GCGGAGACGG GCGCGCGGCG GGGTCCCACG GGCAGAAGAG CCTGGCCTCC AGCGCCCGGC 1020 GCCCGGTTCG CTGCCTCCGG AGCCCCCAAG AGCCTCTCTG AGGGCGGGAG CGGTAGCGCA 1080 GGCCACGCCG ACGGCGACCA CAACGCGCCT GCGCCAAGCC CCGGCCCCAG CGTAACCTCG 1140 TGGGTGACAG TGTGACCTGG GTTTTCTCCG ATACGCGCGA TGTGCCCGCT GAGGGCAATA 1200 TAGCACCCCC CTCGCACCTC ACCCTTAGGC GTGCCAGGCA CTCTTCTAAA TCCGAGCTTC 1260 TATTAACCCA TTTCCTGTCC TGCATCACTT TGCAAGGTGG 1300
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