Tag | Content |
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EnhancerAtlas ID | HS183-01803 | Organism | Homo sapiens | Tissue/cell | T47D-MTVL | Coordinate | chr16:70166460-70168010 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr16:70167243-70167258 | TGAACTCCTGACCTC | - | 6.22 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TTCTTGAGAC GGAGCCTTGC TCCGTGCTCA GACTGGAGTG CAGTTGCACA ATTATAGCTC 60 ACTGCAGCCC CGAACTCCTG GTCTCATAGC TTTTTTTTTT TCTTCTTTTT GGTAGAGACA 120 TGGTCTCGCC ATGTTGCCCA GGTTGATCTC GAACTCCAAG GCTCAAGTGA TCCCTTTCAC 180 CTTGGCCTCC CAAAGTGCTA AGATTACAGA TGTGAGCCAC TGTACCTAGC CCTTTGTGTG 240 TGTTTAGTCA TCTCTATCAT TTTGTGTGTG TGTGAGATGG CGTCTTGCCC TGTCACCTAG 300 GCTGGAGTGC AGTGGCATGA TCATAGCTCA CTGTAGCCTC AAATTCGTGA GCTCAAGCAA 360 TCCTGCCACA TCAGCCTCCC AAGTAGCTGG GATTACAGGT GCTTGCCACC ATGCCTAGCT 420 AATGTTTAAA TTTTTTGTTG AGATGGGGTC TCGCTGTGTT GCCCAGGCTG GTCTCGAACT 480 CTTGGGCTCA GTCAATCCTG CCTCAGCTTC CCAAAGTGCT GTGATTACGG GCATGAGCCA 540 TGATACCCAG CTGCTTTTTT TTTTTTTTTT TTTTTGAGAT GAAGTCTCGC TCTGTTGCCC 600 AGGCTGGAGT GCAGTGGTGT GATCTCGGCT CACTGCAACC TCTGCCTCCC CGGTTCAAGT 660 GATTCTCCTG CCTCAGCCTC CAGAGTAGGT GGTAGGTGGG ATTACAAGCG CCTGCCACCA 720 CTCCCGACTA ATTTTTGTGT TTTTAGTAGA GACAGGGTTT CACCATGTTG ATCAGGCTGG 780 TCTTGAACTC CTGACCTCAG GTGATCCGCC TGCCTCAGCC TCCCAAAGTG CTGGGATTAC 840 AGGCATGAGC CACTGCGTCT GGCCTTTTTT TTTTTTTGAG ATAAGAGTCT TGCTCTGTCG 900 CCCAGACTGG AGTGCAGTGG CACAATCTCG GCTCACTCCA ACCTCCACCT CCTAGGTTCA 960 AGTGATTCTC ATGCCTCAGC CTCCTGAGTA GCTGGGATTA CAGGCATGCA TCAACATGTC 1020 CAGCTAGTTT ATGTATTTTT AGTAGAGACA GGATTTTACC ACGTTGGCCA GGCTGGTCTT 1080 GAAATCCTGG CCTCAAGTGA TCTGCCTGCC TTGGTCTCCC AAAGTGCTGG GAGTAAAGGT 1140 GTGAGCCACT GTGCCCAGCT CTGCTTCTTT TTTTTGTTTT TTTGTTTTTT TTTGAGATGG 1200 AGTTTCACTC TTGTTGCCCA GGCTCAAGTG CAATGGTGCG ATCTCGGCTC ACCGCAACGT 1260 CTGCCTCCCG GGTTCAAGTG ATTCTCCTGC CTCAGCCTCC TGAGTAGCTG GGATTACAGA 1320 CATGCGCCAC CACGCCTGGC TAATTTTGTA TTTTTAGTAG AGACAGGGTT TCTCCATGTT 1380 GGTCAGGCTG GTTTCGAACT CCTGACCTCA GGAGATCTGC CCGCCTTGGC CTCCCAAAGT 1440 GCTGGGATTA CAGACGTGAG CCACCATGCC CGGCCCCTGC TTATTCTTTA TTCACCTAAA 1500 ATTATTGCTC AGATTTTAGG TTTTAGGAGG AGACTTCTTT CAGTAGGACT 1550
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