Tag | Content |
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EnhancerAtlas ID | HS197-03530 |
Organism | Homo sapiens |
Tissue/cell | ZR75-30 |
Coordinate | chr11:17670770-17673180 |
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) |
Crx | MA0467.1 | chr11:17672044-17672055 | TTAATCCTCTT | - | 6.14 | FOXP2 | MA0593.1 | chr11:17672276-17672287 | TTTGTTTACAT | - | 6.14 | GFI1 | MA0038.2 | chr11:17673026-17673038 | GGCAGTGATTTG | - | 6.04 | Nr5a2 | MA0505.1 | chr11:17672094-17672109 | ACGTTCAAGGTCAGG | + | 6.68 | RREB1 | MA0073.1 | chr11:17671600-17671620 | ACACAACACACACACACACA | + | 6.19 | ZNF263 | MA0528.1 | chr11:17672523-17672544 | TGGGGAGGTAGAGGAGAGGGG | + | 6 |
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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 |
GH11I017648 | chr11 | 17669580 | 17676202 |
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Enhancer Sequence | GATTTAAATG TAAAATACAC ATCTCCTTTA ACTAAGTCAT CCTATTTCTA GGTAGCTATG 60 GAAGGCTGAA TAGTGGTCCT CCAAAGATGT ACAAGTCCTA ATTTCTGGAT CTTGCGAATA 120 TTTATATTAC ATTACATGGT AAAAGGGACT CTGCAGACGT GATTAAGGAT CTTGAGATAA 180 GAGGATTATC CTGGGTCATC CAGGTGGGCC CGGTGTAATC ACAAGCGTCC TTATATAAGA 240 GAGGCAGCCA GGTCAGAGTC AGAGAGAGGA GACGGGATGA CAGAAGCGAG GTTGGAGTGA 300 TGTACTTTGA AGTTAGTGTA AGGGGCCACT GGTCAAGAAA TCCAGGCAGC CTCTGGAAGC 360 TGGAAAATCA AGGAACTGGA TTCTCTCCTA GAGCCCCCAG AAGGAACACA GGCTGGCTGG 420 CCCCTTGATT TTAGCTTAGT GAAGCTGATT TCATACTTCT GACCTCTACA ACTGTAAGAG 480 AATAAATGTG TGTGTTTTAA GCCACTAAAT GTGTGGCAAT TTGTTACAGG AGCAATAGGA 540 AACAGATAGC ATCAAAAGAA AGAATTCCTG CAGAGGCATG CGCCAGGATG TTTATTGCGG 600 CATTGTCCTG AGTGTTAAAA ATTAGTAACA ACTGCAAATG CCTGTCAGTA GGGAAGGATT 660 AAGCAACCTG GTACAGCCAC ACTCGTGAAT ATTATGTAGC CCTTTTGGGT ACTGACATGC 720 TGAGCTCTCC AGGATATGTT AAATGATGAC AGGAAATTGT GGGTTGTTTC ACACAGAATG 780 ATCCCTCCTT TATGCACCTG TGTGGGTAAT ACACACACAC ATACAACACA ACACAACACA 840 CACACACACA CACACACACG TCTCATTCCC TTGAAGAGTT TTCAAGATTG AGGAAGGTCC 900 TTCCTGGCTG TTGAGCCACC AACTAGTTCA GTGGCAACTT TGGTCCTAGA ATAGCCTTTT 960 CAGATCCCAG GAGATCATCA GAAGAGACTA GAATAGACTG AAGGCCCTAG GGACATCTGT 1020 GGCATCTCCC CCATTCCTGT TTCCTCCCAC ACTCTGTGCA TTACTTAAAG CTTGAGGCAA 1080 CTCCAGTGGC CACACACAGC TGAGGAAACA GAAAGCCAGG ACCAGCAGAG CCACTGAGAG 1140 ATTGGTGGCC GAGCAGGGTG GCTGCCCAGC TTGCAGCCCC CTGTGACGTA TTTGCAAACA 1200 CGAGGAGTTT TGAGCTGCAG AACCATCCCA TTCTCCGTGG TGCAGGCTCA AGTTCCCGCC 1260 CTGATTTTCT GGGCTTAATC CTCTTCCTGT GGAAATCAAT AAGGACATTG TGATGGAATG 1320 ATTCACGTTC AAGGTCAGGC CGGAGCAAAT TGGAGGCGAC ATGCTGATTT TACTACCCTC 1380 ACTGTGAGGA GAGCCAATCC TGCTCACAGA CCCCCTTAAC CCTTTCCTTG TCACTGTGGT 1440 AAGCACTGTC TGCACAGGCC CCCTCCCCAG GCCCAGATCC CCCTGGCCTC ACCCACGTGT 1500 GGCGCTTTTG TTTACATTTT CCCAAGCCTC TGACCACACA AGGCCTTGGA GTCTTGCACA 1560 CTTGTCATGG TGGTTTGGGG AAGGCAGACG ACAGGTTCAG GAACAGCTTC AAATTGGAAG 1620 TCAAACGCTA CATATCTAAC TTCAGCTTCA TGGGTAACAT CCTGTTCCTC TCCCTTCACC 1680 AGAGCTGTTC CCCTTCCAAC CCTCTTTTCT GAGTTCCAGA CCCCTCTTCC CTGCTTTTCT 1740 GGGTTGTCCC ACATGGGGAG GTAGAGGAGA GGGGACCAAA TTCCTCATTT ATTTTTTTCA 1800 CACACAGCAA GGCTCAAACA TGATAGAAGC TTATTCCTTC CTCCTATTTA AAAAAAACAC 1860 TCAAAATAAG TAGGTAGCTA GAGCTTTGTG TCCAGAATGA TTTAGGGATC CTGGCTCCTC 1920 TGTCTTGAGG TTCTACCACC TTCAGCACGG GCCTCCCAGA GTCTCTGTGA TCTCAGGCAT 1980 CAGCCAGCCG AGGTGCAGGG AGAGCATGTG CGGGAAGCTT GCAGGGCCCA GGACTGAAAG 2040 TGGCTCACTC CCTTCCACTC GGATTCCACT GGCCTGAACT GGCCACATCT CAGTGCAAGA 2100 AAGGCTGGGG AACGTAGTCC AGCTGTGTGC CCAGGAAGAT GGGTCTGGTG GGCAGTGCTG 2160 TCTCTGTGAG GAAGCGGAGA GAGTGAGGAG GACAATGCTA GAAAGTGTGA CTGGAAAAGA 2220 AGAGATAGAG CATGAGTTAG GGGAGGACTT GAGGTAGGCA GTGATTTGAC TGTATGCCCT 2280 GGAGAAGCCA GTGGAAACAG AAAAGCTTTG CTGTGGAGAA AAGTCAGGGT CTCAGAGGGC 2340 CATAGCTGGC ATGAGGAGGG ACAGTGATGA CACAGATACC TCTGGCTGGG CAGACCCCAC 2400 CTTAGGTCTT 2410
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