Tag | Content |
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EnhancerAtlas ID | HS130-26721 |
Organism | Homo sapiens |
Tissue/cell | MDA-MB-231 |
Coordinate | chr8:126524940-126526160 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL2 | MA0478.1 | chr8:126525437-126525448 | GGGTGACTCAG | + | 6.02 | JUNB | MA0490.1 | chr8:126525437-126525448 | GGGTGACTCAG | + | 6.02 | NFKB1 | MA0105.4 | chr8:126525448-126525461 | AGGGGAAGCCCCT | + | 6.02 | NKX2-3 | MA0672.1 | chr8:126525882-126525892 | TTCAAGTGGT | - | 6.02 | RREB1 | MA0073.1 | chr8:126526113-126526133 | CCCCAAACCAAAACCACAGC | + | 6.94 | ZNF263 | MA0528.1 | chr8:126525642-126525663 | GGAGGAGGATGAGGGTGTGAA | + | 6.64 |
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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 |
GH08I125511 | chr8 | 126524044 | 126528513 |
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Enhancer Sequence | AATCAGAAAC TCTGGAGCTG GGGCCTGAGC ATCGTGTGTG TTCCAAGCTC CCCCGTTTGA 60 CTCTGTGAGC AGCGGGAAGT GAAACACTGG AGGAGTGGGA AGGTTTGAAG GGCAGCAGGG 120 GTGGAACCAA CCTCTCTATC CTCTCCGTCC ATCTCTGCCT CTTGCCTAGC CTTCTAGCAG 180 CGTCAGCCTG TAGCCTGTCC CACACCAAAC ACCCGAATCT GCAGAAAGAG CAAATCAGCC 240 CTGTCCCCTT CTTCCTTTTT ACAGACCCCC ACAGCCAGAG GGCAAGAGGC AGGGGTGACC 300 CTAGGCCCTG GGAGATTTTG TTTATGGTGC ATATTTCACT TCTACAGGAT CCTCACAGCT 360 GTGATCTTGC CTCATCGCAG TTGCCAACAC TGAGGGGCTG CCTTCACCCC ATTTGCTAAT 420 TCCCCAAGTT CCTCTTTCGG GCATGTTCCT GTCCCTCCGT GTTCCCGTGG CCGCGTGGAA 480 ATGGACCGAG GCCCACAGGG TGACTCAGAG GGGAAGCCCC TGCGCTGCGA GGCTCCCAGC 540 AGCTCCTGGA TTGCGTAAGG GCTATTTTTG AGGAGATTGC AGACGATCTG ATGAATCATA 600 GCAAACACAC ATGGCTCCGG CGGGGGACAG CCCTTCCTCA TGTTGCTGTG GAAAGTGGAG 660 CTTCTCAAAA TGAATCAGCA GAGCCTGAAC CCCAGGTCTG TGGGAGGAGG ATGAGGGTGT 720 GAATTACACA TTTCCAAAGT ATTGGGGTGC GGTCGCCTGG ACCTGGGAGC GGGGGCTGCA 780 GGGACCCAAG TCTTTGGTTT TCTCAGTGAC TCAAAGATCC TCTCTCACCC ACCTGAGCCT 840 GCCATTTGGA ATCTCCTGAC CCTCCATCAG TCTAGAGCAA TCACTTGCAC TTCCTGGGGT 900 CCAGGGAGAA AGTTAGGGTG GGCGCAGCCT AGTGTAACTG CTTTCAAGTG GTGGCACACA 960 GGGTCTGAAT CCAGAAATCC AGAGGCCACC CCTTCTCTGG GTTGCCCATA TGAGAAATTC 1020 CTGACCACGA GGAAAAGGCT CAAATTACAC CTGCTAGGGG TAGGGGAGGC CCCCCTTGCT 1080 CCCCCAAGCT CAGCGGCATG AGAACTAAGG GGGAGAGTGG AAGGGTGGTT GGGAGTCGTC 1140 AGGCTTTAGA ATCGGACAGT ATTGGATTTG AGGCCCCAAA CCAAAACCAC AGCTTGGAAA 1200 AAGTCCTAGG ACATAGCTGA 1220
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