Tag | Content |
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EnhancerAtlas ID | HS129-36709 | Organism | Homo sapiens | Tissue/cell | MCF10A | Coordinate | chr8:145676150-145677740 | SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SP2 | MA0516.2 | chr8:145677493-145677510 | AGGTGGGCGGGGCTGCT | - | 6.39 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CCTCTGTGGA GACAGACAGG GCCGGAAAGA GCCGGCTGTT AGTGTGGGCA GGGCTGGGCA 60 GCAACGCCTT CCCTGACCAG GCCGAGGGCA GGCTCAGCCG GGGAGGAAGG CAACTTACCC 120 GGACACCGGG CTCTGCTTGT CACAAGCAAG CCAAACGCAA CTATGGCAAA TGGAGGTGCA 180 CACAAGCTTT GAGGGGAACA ACCACAAACA GAATCAACAT GGATTAGCTG GAGAGTCCAG 240 AGGCTGCACG TGTCAGGCCA CACCCCAGGC GTGCCCGACC CACGCTGGCC TCCCTCACCG 300 CCCCGAGCCC CGGGTGTCCC CCAGGGCGGG GTAAGCAGAC ACACAGACAG GATGCGGTTC 360 CGAGAACAAG TGCACTTTAT TGGTTCTGAT ACAGAGGAGC TGCCAGAAAA GCCAGCAGGC 420 GGCTGCGGCA CCCAGCCCTG CCCGAGGGGA GCACCAGGTC TGCAGGCACC GGGCCTGATC 480 CGGAGCTGCC AATCAGCAGG CAGCCCTGCC TGCACAGTCC TCTTGGGCAG CCCACAGCCT 540 GTGGCCGGCA AGTCCCTCCG TGGAGGCGTG GGTTCCCAGG TGGCCAGTCT TTCCTGCGCG 600 AATGGGGCTT CTCACCTGGC CACGGCCACA GCCACAGTGC CCCAGCCTGC CTAGACTCCA 660 CGAGGCCCCG GTATCTCCAG GACAGCTAAG GCTGCTACTC ACCACGGGCT GTGGCTGCCG 720 CAGAGACCCC AGGCCCTCGG CCTCTCTGGC CTGCTCGGGC CCACATCCCG CTGGGCACAG 780 TCCAGGCAGC AGGGCGGGAC TGGCTGCCCA CGACCACCCT GCTTGCGCCA CGCCTGGTGC 840 TCTGAGCTGG CCGCCTGGTG TGGGCTGAGA GTAGAGGGAT GGAGCTTCCT CCAGTGGCCC 900 CAGCATCAAC AGGTGCTTCT CGCTGTCCTC TGGGCCAGGC TCTGGCCTGG CTCCTGCTCC 960 CCGACACGTT CAAAGGCGGT GGCAGCGGCC CAGAGAGCCA CGAGATCCAG TGTGCCTGCG 1020 CACGCATCCA GCCTGGGCGT CTGTGGGTGT CCACTCCCGG TTCTACAGTT TGAGTCGGGC 1080 ACCCTCAGCT TGTTGTGGAG CCCTCTCCCT GAATGGCTTC GTGCCAGCCT TGAGAGGCCC 1140 ATGGCCGGGG CAGTGACTGC CTGCAGGTAG GACCTCACTC GGCAGGGTGC TCTTCTTGCC 1200 CCAGGGTCCG AGGGGCAGGC CCCTAGCTCC CAGGCCCCCT GAGACCTGCC CACTTTCTGG 1260 TTAGACCCTG ACTGTCTTGA GGCTCTGGAG CCCCACAGTG AGATGCCACC TTGCAGGGAT 1320 GGTGAAGCCA GGGTGGCGAG GACAGGTGGG CGGGGCTGCT GTGAGAGCCA CACAGGTGTG 1380 CACCTGGGGT CTGCCTCGGC CCCTCCTTCC ACTCAGTCTC CGGCCTGTCT TCTCGACCGA 1440 GGTGTCCACC TGTCCACCGG GAGCTTGTCC AGAGCCCGGC TGTCCGGCGC TGTCAGTGCC 1500 CAGTGCCCAG AGCCTGCTGC CCCCAGACTC CTGGCTGCCA GCCCCCCAAC CCACACCTGT 1560 GTGGCATGCA GCAGGCGGCG GGGCGCCTCA 1590
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