Tag | Content |
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EnhancerAtlas ID | HS128-04512 | Organism | Homo sapiens | Tissue/cell | MCF-7 | Coordinate | chr12:8827540-8829270 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXP1 | MA0481.2 | chr12:8827978-8827990 | TTCTGTTTACTC | - | 6.27 | NKX2-5 | MA0063.2 | chr12:8829225-8829235 | CTCAAGTGGT | - | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| | Number: 1 | ID | Chromosome | Start | End |
GH12I008675 | chr12 | 8827797 | 8828996 |
| Enhancer Sequence | CCTCCACCTC CTGGGTTCAA GCAATTCTCC TGCCTCAGCC TCCCGAGTAG CCGGGATTAC 60 AGGTGCCTGC CACCACACCC AGCTAATTTT TGTATTTTAG TAGAGACAGG GTTTCACCAT 120 GTTGGCCAGG CTGGTCTTGA ACTCCCAACC TCAGGTGATC CACCCACTTT GGCCTCAAAA 180 TGCTGGGATT ATAGGCGTAA GCCACCACAC CTGGCCCTTT TCTCACAATT TTAAGAAAAG 240 CTGTCACAGA AGAACCTCTT TGTTGCTGAA TAATACAGAC ACATTTCAGT CTTATTTTCT 300 TATTTTCTGA AACATTAGTC ATTGCTGACC AGTCCCTACT TTTGAAATGT CCCCTCCTCT 360 TGACATCTAT AATATCACAG TCCTTGTCTT CCTCTTAACA CCTCTCTACT GTTCTTTTAC 420 ATTTCTTTTT TCTTCTTCTT CTGTTTACTC TTAAGTGCTG GTTTTCAAGG TTTTGGCCCG 480 GCCACCTCTC TTTTTACTGT ACTTTCTCCC TCTCCTTAAT CCACTCCCAA CTCTTCATTT 540 ACCATCTATT GGTTTATTCT CCCAGATCTA TGCTTCAGTC TAACCTCTAT CTATCACCTA 600 AAATAATCAA AAGGGTCAAG ATCTAATTTC AAAACAGTTT ATTCTGGTAC AAAGAGTGGA 660 AACATCAACT CCAAAAGAAG GAAGTCAGCT TTGTGAAGTC AGGAAGTTAA GGGTTCATTT 720 ATATAGACAG AGGAGCCTTT AGCAGGATTA CAACTTTTTT TAGACAAGGT TGGCACATAG 780 TTATAGCAAA CTGATTGGTT ATAAAAGTGT TTCTTTTTGG GAGAGTACAT ATAGTTGTTT 840 TCTTGTTTTT CTTTTTTTTT TTTTTTAACG GAAGTGTAAT AGTCATGGGT TTTCTGTCAT 900 CTGGTCTAAG CAAGGCAGAA CAACAAAGAA AAAGTTAATC TGTAACAAAG GTCATTAATT 960 AAGAAGGCAG GAGGTTTTTG TCCCTGACGT CGTTAAATTT TCTCTAGTCA TTGTGCAGGA 1020 CAAGAAAAAT AAGAAAACAA GTTAATCTAT AATCTGAGAA ACATGCTATA GCCATATGTG 1080 ACTCAGATCA ATCTCATCTC TGTCAAGGTT TAAATGTTTT GGGGGGTTCC AACAGCTTTT 1140 CTTTTTGAGA CAGGGTCTCA CTTTGTCACC CAGGCTGGAG TGCAGTAGCG TGATCTTGGC 1200 TCACTGCAGC CTCGACCTCC TGGGCTCAAG CTATCCTCCC ACCTCAGCTC TCCCAGTAGC 1260 TGGGACCACA AGCGTATACC ACCACACTCA GCTAATTTTT TGTATTTTTT GTAGAGACAG 1320 GTTTTCACCA TGTTACCTGG GCTGGTCTCG AGCTCCTGAG CTTGAGTGAT CCCCCAGTCT 1380 TGGCCTCCCA AAGTACTAGG ATTATAGGAG TGAGCCACTG TGCTCAACCC CCAACAGCTT 1440 TTTTTTTTTT TTTTTTTTTT TTTTTTTTTT TTGAGACAGA GTCTTGCTCT GTTGCCCAGG 1500 CTGGAGTGCA GTGGCATAAT CTCGGCTCAC TGCAACCTCT GCCTCCCGGG TTCAAGTGAT 1560 TCTCCTGCCT CAGCCTCCTG AGTAGCCAGG ACTACGGGTG TGCACCACCA CACCTGACTA 1620 ATTTTTGTAT TTTTAGTAGA CACGGGGTTT CACCATGTTT GCCAGGCTGG TCTTGAACGC 1680 CTGGCCTCAA GTGGTCCACC CGCCTCGGCT TCCCAAAGTG CTAGGATTAC 1730
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