| Tag | Content |
|---|
EnhancerAtlas ID | HS130-02177 | Organism | Homo sapiens | Tissue/cell | MDA-MB-231 | Coordinate | chr1:165566790-165568100 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr1:165568073-165568091 | GGAAGGAAAGAAAGGAGG | + | 6.51 | | EWSR1-FLI1 | MA0149.1 | chr1:165568069-165568087 | AGAAGGAAGGAAAGAAAG | + | 6.94 | | RFX5 | MA0510.2 | chr1:165567420-165567436 | GGTTGCTGTGGCAACA | + | 6.28 | | RFX5 | MA0510.2 | chr1:165567420-165567436 | GGTTGCTGTGGCAACA | - | 6.28 | | ZNF263 | MA0528.1 | chr1:165568070-165568091 | GAAGGAAGGAAAGAAAGGAGG | + | 6.27 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AATGTCCCTT ACAACGGCCA GCCCCAATCC CACCGGGAGT AACTTCGACA TATTCCTTTA 60
CTCTTTCTGC TTCTTTTAAC ATATCTGAAA ATGGAAAGTA GGTAAACTGC ACCTACTTCC 120
TCAGAAGGTG GAAGGGATTC GTGGTGTAAT CTCTCTACGT GGGCGGAAAC ACACTGTAAG 180
CACCCAAATA ACAAAATGTA AATGTCTAGC AAGTATATAA AAAAACATCA GGAAAGGTTT 240
TTTGTTTGTT TTTGTTTTGT TTTGTTTTTG TTTTTGTTTT TCATATAAAA GGCCAAAAGT 300
AGGGAAGTGA CAGAAAGGCT GATTGCCGAC CTTTTCAGAG CTTACTTATT TTAAACAATT 360
ACACTGACTC ATAAAATAAA AGTATTTCTT GTGCCCCGGT CAAAAGCAAG TGGATTTTTA 420
CTTTAAGGGT GAATAATAAG AATGCTTTGG GGATGACGAA TAAAAGGGCT TCCCCCGGCT 480
AGCCGAGGCG GAGCCATCGG GGATATACCA TCTCTCCTCG TCGATCTGGA AGGCTTTCTG 540
AAGGAACTGG GGTTTGTGTC CCTGGCACGC CCGGGACCTG CGTGGGGCTC AGCGCGCTGC 600
CAGGCGACCT CAGCAGCCCA GAGCTTCAAC GGTTGCTGTG GCAACAGGCC GCCCAGAGCA 660
GCAGTCAAAG TCCCTGCGTG AGCGACTGCA CTTCCCAAGC GCGGAGAGTC TGCCCAATGA 720
GTTCCGCCCT CTCTAGCGCG CTTTCTGTGA TCCACCAATC AGGCTCTGCC ACGCCCGAGC 780
TGAGTGGTCA GCTTGCCTGG GAGGGCGGGG TTAGGGTGCA GAAACAGGAC GGAGAAGGGG 840
GCTGTATTTC CCCTGGCGTG TGAAATGGAT GTTAGTGACT AAAGCTCAAT TTTCCAGTTA 900
AGGGAGGAGC CGAGACTTTT AAGTCGAGTG TTCCTGTGGG GCCAAAAGGA TGGTTTCAGA 960
GAAATCCCAG GAAGTGAGAG TGCTGGGATA TGCGAGGGGC CCACGGAGCC CTCCCCTGCG 1020
TGTCTGAGAT CACACCCTGC GGGTACCCTG CCGTCGTGTG CTGAAGGAGG TGACTGGATC 1080
TCGACTCCAG AGTTTGCTCC TGAGATCGAA AAACAAAACA ACCCAATAAT AGTAATGACA 1140
GCCCTGGGTG GGGACAGTTG CAGCAGGTCT CATGAGAAAC TCACTAATTT TGTAGGTTCA 1200
GGGAAGGCGT GGGCATGTTG GTGAAGTAAG GTTCTGAGTG GAAGAAGAAA ATGCTGCTTC 1260
TGGGGAAGAG AATACCGTCA GAAGGAAGGA AAGAAAGGAG GGAGTGGGAG 1310
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