Tag | Content |
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EnhancerAtlas ID | HS180-18358 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr16:28543120-28544680 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
GFI1 | MA0038.2 | chr16:28543320-28543332 | TGCAGTGATTGC | - | 6.14 | NFKB1 | MA0105.4 | chr16:28543618-28543631 | AGGGGGATCCCCC | + | 6.02 | NFKB1 | MA0105.4 | chr16:28543618-28543631 | AGGGGGATCCCCC | - | 6.03 | NFYA | MA0060.3 | chr16:28543830-28543841 | GGCCAATCAGA | + | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr16 | 28543579 | 28543953 | chr16 | 28543196 | 28544167 | chr16 | 28543389 | 28544200 |
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| Number: 1 | ID | Chromosome | Start | End |
GH16I028531 | chr16 | 28543123 | 28546830 |
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Enhancer Sequence | TAGCATTAAC TTTAGGGGAT TTTAGTTAAA AAATCAATTT TGGGGCTGGG CACGGTGGCT 60 CATGCCTGTA ATCCCACCAC TTTTGGAAGG CCGAGGCAGG AGGATCACTT GAGGACAGGA 120 GTTTGAAACC AGCCTTGGCA TCATAGCAGC GAGACTTCAT CTCTACGAAA AATTTAAAAA 180 TTAGCCCAGG AGGTCAAGGC TGCAGTGATT GCACCACTCC ACCCCAGCCT GGGTGATAGA 240 CTGAAACCCT GTCTCAAAAA GGAGAAAACT GAGGGTGATT CTGAAATTTA AAAATGTACT 300 CCTGTATCTG TGAGCTGGCC TTTGAGAAAG GGGAAGGTGG AAGAGAATCA GGTTGCTTGC 360 AGAACAGACA GACAACCCCA TGGTGAGTTT CTCAGTTCTC TGCAAGGAGT CGGGAGTCCT 420 TTGAGTTACA GAAGCCTGAC AGGGCCAATT CTGTAAGCCC CTGGGGTAGG ACAGAGGTCA 480 GTGATTTCTC TAGTTCTCAG GGGGATCCCC CCAAAATGGG GAAACAGACA TGCAACCAGA 540 AGAAAAAGAA AGGGTTTAGG AAAGGGGATG GAGACAGAAG AGGAAGAGTC TGGGTAGGAT 600 CCTTTCGGAT CCAAAAATTC TGCAATTCCA AGAATTGCCT TAATTCCCAG AACAGCCACT 660 TAAAGGCCTC TCAGGCAGAG GCTGTGCCAG GCGAGGGCGA GGCCAGGAAA GGCCAATCAG 720 AGGCCAGGAG GGAGGGGCAG TGTGTGAGGA CTCCTGGCTG GTGTCAAAGG ACCCAGGACA 780 GGGAGTGGCC ATTCCAGCTA GGGACACAGT GCTTCCCAGC CTTCATTTTC TCTTTTGACA 840 GAAGAGAGGC CAGTCTCACC ATTTGACAGG TGAGGAAACC CAGGCCCAGA GGAGTAATTG 900 ACCAGAAATT AACGAGAGTT TAGGATTCTT CATTGTCAAT ACATGGTTCT TCCCAGGCAT 960 GTAGCAAAGG GGGAAAAATC CAGGCTTTAA AATTCAGATA GACCTGAGTT CATAATTCCA 1020 AGTCCTACAG GATGTGGCTG TGTGACTTTA GGCAAATTAC TTAATGTCTC CGAACCTCAG 1080 TTTTCCGGTC TGAAAAAAAG GGGATCATTA ATAGTATGTC CTATTGGGTT ATCGTAAGGA 1140 TTAAATGGAG CAAAGCCTAT AAAACACTTC TCACAGAATA GGAGCTCCAA ACACAGCAGA 1200 GATGTTTCCA GGATTTTCTG AAGCCAACAC ACCAGGTCTG TGCTGGGCTG AGGGCCGACT 1260 GCCTGGTGTT GCTCCTGCCA TTTGCTCCCT GGGTTCTAGA GCTGATGGTG GCCCTATTCC 1320 TGGTTCCAGT CATATCAGGA TTCTATTTGT CCCTCTCAGC AGCACAGGCC TCCAGCAGCA 1380 TCCTGGTAAC TCAGAAGGCA TCCAATAAGC ATTGATTGAG TTAATATGTA ACTTGTATGG 1440 AAAGAGGAGT TGGAGGCAAA ATCTGAAGGA TTTCCAAGGT AGACTGTAAG ATTCTGGGCC 1500 CAGGCTTCCG TGTGATCCCA GAGGAGGGTC GGCCTGGGGT GGAGGTCAGG AGATGGGTGG 1560
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