Tag | Content |
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EnhancerAtlas ID | HS184-13444 | Organism | Homo sapiens | Tissue/cell | T47D | Coordinate | chr17:38089990-38091130 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr17:38090203-38090224 | GGAAGAAGGAGGGGGAGGGGA | + | 6.08 | ZNF263 | MA0528.1 | chr17:38090053-38090074 | CTACTCCTCCCCTCCTCCCCC | - | 6.16 | ZNF263 | MA0528.1 | chr17:38090050-38090071 | CTCCTACTCCTCCCCTCCTCC | - | 6.4 | ZNF263 | MA0528.1 | chr17:38090062-38090083 | CCCTCCTCCCCCACCTGCTTC | - | 7.31 | ZNF263 | MA0528.1 | chr17:38090207-38090228 | GAAGGAGGGGGAGGGGAAGGC | + | 7.53 | ZNF263 | MA0528.1 | chr17:38090204-38090225 | GAAGAAGGAGGGGGAGGGGAA | + | 7.87 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AAAAGAAAAG AAAAAAGAAA CAGAGCCCCT TCCCCTGGGG GAAAGAATAC CACCTCTCCA 60 CTCCTACTCC TCCCCTCCTC CCCCACCTGC TTCCTGAAGG GAGGGTGGTG AGGTCCTGTC 120 CAGAGCAAGT GCAAGGAAGG AAAGAACTGC TTATTTCATT GACAGTTGTG TTTTTATTTT 180 TGTTTGGGTG GGGGATACCC CAGGCATGTG GTGGGAAGAA GGAGGGGGAG GGGAAGGCAG 240 ATGTTAAGCA GACAAAGGAG CAGCGAATGA CCCTCCTGAG AACTACTGAG CCAGTCAGAA 300 GCCAGGAGTG GGTGCGGGAC TGGCAGCATC GCCAGCGGGC ACTCTGTTCT GCCTCCCTCG 360 CCCAGTCCTG TAGTTGGCTA TTTTGGGCTG TGGAGAGAAA GGGCTGAACT GGTCAGGGCC 420 ACTGGGTCCC CATCCCCCAG CCTGTGCCTG GGAACAAGAA CCTCCCTGGG GAACCAAGTG 480 CAGGGAGGTA CCTTAGGAAC CCTTCAACCT GCATATTCTT TGATATGGAC AATTGACACT 540 CTCCCATGAA CAAAAGCAGT TAGAAAACTG AAAATATTTC AGATCAAAAG GGCAATGGAT 600 ATAAAAACAG TAAGTTCAAG ACAAGACCCC CTAGCTCCCT ACCAACTGAG TTCCTACTCC 660 TAGCCTCACC TGTCTAGAAA TCTGGGTGGC CACCGTTCCC AGATCACCTT CTTCTGCCTA 720 AGGCCAGCTC CTCCCTCAGT AACAATCACA GCAAACATTA TTGTTTGCTA TGTTCCAGGC 780 ACTGGGCAAA GGGCTTTATT TGTCTGTTAC AGAACCACCT CCCCCTGGGC TGCTAGACTT 840 GCTCCCTGTC TCACATTTGC ATTTCCCGAA CAGAGTGAAT TCTCAATAAA TGTTAACTGA 900 ACTATGTAAC GGAACTGTTA CCAGAAAGGG GTCCCGATCC AGACACCAAG AGAGGGTTCT 960 TGGATCTCAC GCAAGAAAGA ATTCAGGGTG AGTCCACAGT GCAAAGTAAA AGCAAGTTTA 1020 TTAAGTAAAG GAATAAAATA ATGGCTACTC AACAGACAGA GCAGCCCCGA GGGCTGCTGG 1080 TTGCCCATTT TTATGGTTAT TTCTTGATGA TGTGCTAAAC ACGGGGTGGG TTATTCGTGC 1140
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