Tag | Content |
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EnhancerAtlas ID | HS093-29403 | Organism | Homo sapiens | Tissue/cell | HL-60 | Coordinate | chr7:158465480-158466140 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFE2L1 | MA0089.2 | chr7:158465875-158465890 | GAGTGACTCAGCAGA | + | 6.62 | Nfe2l2 | MA0150.2 | chr7:158465873-158465888 | GTGAGTGACTCAGCA | + | 6.08 | Nr2f6(var.2) | MA0728.1 | chr7:158465723-158465738 | GTGGTCAGAAGGTCA | + | 6.14 | ZNF263 | MA0528.1 | chr7:158465907-158465928 | GGAGAAAGAGGAGCAAGGGGG | + | 6.18 | ZNF263 | MA0528.1 | chr7:158465916-158465937 | GGAGCAAGGGGGAGAGAGGAA | + | 6.2 | ZNF263 | MA0528.1 | chr7:158465913-158465934 | AGAGGAGCAAGGGGGAGAGAG | + | 6.79 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GCCACCGGCC ACCACCTACC TTGCCAGTTC CCCCAATCCC ACAGCCCCTG TAGCCCCTGC 60 CATAACACTG TGTTCTCCTA ATTCTCCTTC AACTTCTCTG GTCTTTCTTC TGTAGATTCT 120 CTGCTGACTC TTCCTCTACT CCAGAGCCCA CTCATCCCTC CTCACAGATG ACCCATCTGG 180 GCAAGGGAGG CATCTCAGAG TGGCCCTGCA AGGGTTTCCT CAGAAGCATG AAAGCACCAG 240 ACGGTGGTCA GAAGGTCAGG ACCAAGAGAA GACCGGCCAG GGAGCTGCAG CCACTTTGGA 300 TGACAGCAAC AGGAAGGAGC AGGTGAACCT CAGACACCAG GAAGGGAAAG ACAGGACTTG 360 GGTGAAGGAG GAAGAAGCAA GAACAGCACG CAAGTGAGTG ACTCAGCAGA TGGCATCATC 420 ACTTCAAGGA GAAAGAGGAG CAAGGGGGAG AGAGGAAAAT AAATAAAACT CTTGGATGGC 480 AGCAGGTTTG GAAAAGATGG TCATCAACTC AGCAGTGGAG ACAGGGTGGT TGCTATGACG 540 TACAACCAAG GCCCCATCAG AAATGAAGCA CTCACCCCAG CTGTCCTGGG GCTGCTGAGC 600 TGCCCTCGCC ATCAGCATGC TTGGGGATGG CCTCCTGAAG AAAATGCCTT CTTCTTCCCG 660
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