Tag | Content |
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EnhancerAtlas ID | HS012-14570 | Organism | Homo sapiens | Tissue/cell | Caco-2 | Coordinate | chr17:38108220-38109220 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SP1 | MA0079.4 | chr17:38109077-38109092 | TGTGGGCGTGGCTGG | - | 6.21 | SP3 | MA0746.2 | chr17:38109077-38109090 | TGTGGGCGTGGCT | - | 6.37 | SP4 | MA0685.1 | chr17:38109075-38109092 | GGTGTGGGCGTGGCTGG | - | 6.36 | SP8 | MA0747.1 | chr17:38109077-38109089 | TGTGGGCGTGGC | - | 6.22 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CATCCAAGAA CAAGAAGCTG AAAATGCCCT CAGAAGGTCA GAGAAGCAGA GGGCTCTTCT 60 CCCCATCCCC AACCCAAAGG TGGACAAAAC CTTAGAAGGT GAGAGGGACA CAGAGACCCC 120 TTTCCTAAGC AAAGGAAAGA AATCTGTCAA GTCAGCAGCT GAAGCCCAGA GCCCCTTCGC 180 AAGGGAAAGA CTTTGGGGTG ATGGTGGGTG GGATGCAGAG GGGTCCCCTG GACATTGGCG 240 GGACGTAGTG CTGACTGTGA TGGCAGCCAC GGGTTTCTTG GGCCTTTTCG GTGCATCCTC 300 CCCGCAAGCC TCCACCACGC TGTTCCAGGT AGGCTGAGGT TAGGCCCACT CAGGGCGGCA 360 CCTTGGCGCA GGACACCTCT TCCGTTTGGG CTTTCCGTCC TCGTGATTTC GCTCTCCATC 420 TGACAGTCAT CCATGGTGAC AGGGTGTGTC CCTTTCCCCT AAACAGGATC CTCAATGCCC 480 ATCGGAAAAC GTTGTAAGGC GTTGAGCCCC CAACGCCCCC TCACCACAAG ACCCTGCTGT 540 GACCATCTTT TCCTGGTGAG GAGAGTCTGC ACGGGGGAGC AGGGCGCCAT ACCCCAGAAA 600 GAAACCTCTG TGCCTGGGAG TGAGGGACTC GCTGAGTAAA GTGAGGTCGA AGAGGGTGGA 660 GAGGGGTAGG GTCCCAGTCA CCACTGTCCT GAACCCACAG TTCAGTCCGG GCCCAAGATG 720 GCCCCACAGG AGCACAGGGG GTTTCGGGCG CTGCAGGTGG AGGTGAAGGA CCAGCTGCGG 780 TGCGGAAAGG CCTGACCCGG GCGGCAGATC GCCTGCGGAG AGAATGACCG GCTGGGGTGG 840 AGGCGGGGCT GGGGTGGTGT GGGCGTGGCT GGGGAGGCGT GGCTGGTGTG GTAGGCTTAA 900 GCAGTGAGGG CGGGACTGGG GCAGAGGCGG GGTTTGGGCG CTGAGGGCGG GGCTGGGGCT 960 TTGAGGAGGT GGCTGGGGCT GGGGCGAGGC TGGTGCGGAG 1000
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