Tag | Content |
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EnhancerAtlas ID | HS052-36203 | Organism | Homo sapiens | Tissue/cell | Fibroblast_foreskin | Coordinate | chr7:158465430-158466820 | 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 | CCACCTGTGT CCACAGCCTC CTCTTGATCC TGCCCTCCCA CTGGACACCG GCCACCGGCC 60 ACCACCTACC TTGCCAGTTC CCCCAATCCC ACAGCCCCTG TAGCCCCTGC CATAACACTG 120 TGTTCTCCTA ATTCTCCTTC AACTTCTCTG GTCTTTCTTC TGTAGATTCT CTGCTGACTC 180 TTCCTCTACT CCAGAGCCCA CTCATCCCTC CTCACAGATG ACCCATCTGG GCAAGGGAGG 240 CATCTCAGAG TGGCCCTGCA AGGGTTTCCT CAGAAGCATG AAAGCACCAG ACGGTGGTCA 300 GAAGGTCAGG ACCAAGAGAA GACCGGCCAG GGAGCTGCAG CCACTTTGGA TGACAGCAAC 360 AGGAAGGAGC AGGTGAACCT CAGACACCAG GAAGGGAAAG ACAGGACTTG GGTGAAGGAG 420 GAAGAAGCAA GAACAGCACG CAAGTGAGTG ACTCAGCAGA TGGCATCATC ACTTCAAGGA 480 GAAAGAGGAG CAAGGGGGAG AGAGGAAAAT AAATAAAACT CTTGGATGGC AGCAGGTTTG 540 GAAAAGATGG TCATCAACTC AGCAGTGGAG ACAGGGTGGT TGCTATGACG TACAACCAAG 600 GCCCCATCAG AAATGAAGCA CTCACCCCAG CTGTCCTGGG GCTGCTGAGC TGCCCTCGCC 660 ATCAGCATGC TTGGGGATGG CCTCCTGAAG AAAATGCCTT CTTCTTCCCG GGCAGCCAGT 720 GTGCAATAGT GAATCAGCAT GGGCCCAGTC TGAAGGGCTC TGCTGGCTCC AGAGCTGCCT 780 GTGGGTCTGC ACGAGGCTTT CCCAGGCTGT GTCACGGCTT AATGTCCCTT CCCTTACACA 840 GGTGTGCACC CCAGGAGCAC TTCCTAATCT GCATGCTGTG GATAGTCTGA ATCTCAGAGC 900 TACCTGCTGG TCACCTGAGC AGAGCTCTCA AAGAAGACGC TTGTCTGTAA ACTGGGACCA 960 GCCGCATGCA AACCACAGTC AGAGCAAGGC TGGAAACCGG ATAGCCAGGG GGAGCCCGTC 1020 ACAGTGCAAG AGGCGCACGG CTCCCTGGCT CCTCAGCCAG CACTTGAAGA GTAAGAGTAT 1080 TCAACCAAAG ACCAGGAGGA AGAAGAGGGA CTGAGGTTTT ACCACAACAT CCAGAGGGAC 1140 AAGGGAATGG TGTAGGAATG AATTCTGCTC AGAGGTCAAA AAAGTCTAGA GAAGTGGTCA 1200 TGTGAAATTC ACCTTGGCTA GAAATGCTTT ACTGGAGTAG TGGACATAGA AGACGCTTTA 1260 TAGTAGACTG GGGAGTTGCA GGAAATGGAG ATAGACTATT TAGGTGACCA CTAAACTAAG 1320 ACTCTTTTGA GAGTAAGAAG GTTGCTCCTA ACAATTACTG CAGAGCAACA GGCATGAGCC 1380 CAAATGTCTG 1390
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