Tag | Content |
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EnhancerAtlas ID | HS147-00570 | Organism | Homo sapiens | Tissue/cell | NHEK | Coordinate | chr1:17617950-17619390 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HES2 | MA0616.2 | chr1:17618127-17618137 | GGCACGTGCC | + | 6.02 | HES2 | MA0616.2 | chr1:17618127-17618137 | GGCACGTGCC | - | 6.02 | SOX10 | MA0442.2 | chr1:17619115-17619126 | AAAACAAAGCA | + | 6.02 | ZNF263 | MA0528.1 | chr1:17619356-17619377 | AGGGGAGGGGAGGGGAGGGAA | + | 6.45 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CTTCTTTAAC CCCATAAAGA ATAGCTATAG GCTGGGTGTG GTAGCTCACT CCTGTAATCC 60 CAGCAATTTG GGAGGCTGAG GTGGGTGGAT CGTTTGAGGT CAGGAGTTTA AGACCAGCCT 120 GGGCAACATG GTGAAACCTT GTCTCTACTA AAAATACAAA AATCAGTGGG GCATGATGGC 180 ACGTGCCTGC AATCCCAGCT ACTCAGGAGG CTGAGACAGG AGGATTGCTT GAACTCAAGA 240 GGCGGAGGTT GCAGTGAGCC AAGATCACGC CACTGCACTG CAGCCTGGGT GACAGAGCAA 300 GATTCTGTCT CAGAAAAAAA AAGGTACAAT AGTGATTCTC AAAGTGTGGT CCCCAGACCA 360 GCATTAGCAT TATCAGCATT ACCAGGGAGC GTGTCCAAAA TGGAAGTCCT CAGGCCCACC 420 CACACCTTCT GAATCAGAAA CTCTGGAGGC TGGGGGAGCA GCAGTCTGTG TTTCAATAAG 480 CCCTTCAGGT AATTCTAGTG CCACTGAAGT TTGAGAACTA CTGATCTATA AGAAACTCAC 540 ATCAAAAATT ATTCTTAATG ATAAAGTATT GAAACCATTC CTTCTAGGAT CAGAATAAGA 600 ATACCCATTA TCATAACTGT TAATCAGCAT TGAACAGAAG GTTCTTGCCA TTGAGGTATA 660 AGATTAGAAA GGAATTATTA TATATACAGA AAATCCAAAA GAATCTACAA AGTAAAAGAA 720 TTCATAAGAG GGTTTAGCGA GGCTGTCACT ATAAAACCAA TATACAAAAA TCAATTGTAT 780 TTTTTTTTCT TGTGGGACAG GGTCTTGCTC TGTCACCTAG GCTGGAATGT AATGGCTCAG 840 TCACAATGTA CTGTAGCCTC GACCTCCTGG GCTCGAGTGA TTCCCCCACC TAAGTCTCCC 900 AAGTAGCTGG GACTACAGGT GTGTGCCACC ATGCCTGGCT ATTTTTTTTT TTTTTTTTTT 960 TTTTTTTGTA GAGACAGGAT ATCGCATGTT GCCCCAGCTG ATTGCAAACT CCTGGCCTCA 1020 AGCAATCCTC CCGCCTTGGT CTCCCAGAGT GCTGGGATTA CAGGTATGAG TCACCACACC 1080 TGGCCCAACT ACATTTCTAT ATACTAAAAA GAAATAGAAA ATGGCAAATT TGAAATGTGC 1140 CATTTATAAG AGCATCAAAA AGTAAAAAAC AAAGCATATC TAACAAAAGA TGTGCAAAAA 1200 CCTTATGGAG CATACTATAC AACTGTATTG AAAAAACATT AGAGGAGATC TAATTAATGG 1260 AGAGATACGC CATATTCATA GATTGAAAGG CTCAATATTA AAAAGATTTC AGTTCTCTGC 1320 AAGACCTACG AATCAGTGTA AATCCAGTCA GAATCTCCAC AGGGTGCGTG TATGTGTGTG 1380 TGCACATGTG AGAGCATGCA CTTGAGAGGG GAGGGGAGGG GAGGGAAATG TGGGAGGGGA 1440
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