Tag | Content |
---|
EnhancerAtlas ID | HS183-13729 | Organism | Homo sapiens | Tissue/cell | T47D-MTVL | Coordinate | chr9:130926200-130928340 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr9:130927315-130927330 | AAGGTCAGGAGTTCA | + | 6.04 | Nr2f6(var.2) | MA0728.1 | chr9:130928065-130928080 | TGAACTCCTGACCTC | - | 6.22 | TP53 | MA0106.3 | chr9:130926521-130926539 | AACATGCTAAGACATGCT | + | 6.42 | TP53 | MA0106.3 | chr9:130926521-130926539 | AACATGCTAAGACATGCT | - | 6.72 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | ACACCGCTGT GCCTCTCTCC TCTGTATCCC AGGACGAGAA CCCCAGCAGC TGCTGGAGGC 60 GAACAGGACT GTCTAGGTGT TCAGGTGTTG ATCCTATACT GGCGGCTCAG AGGCCAGGTG 120 GTAGGGCTGG GGTTCTTGGT CACCTGTACT TCTGGACACA GAAGGTGCAG GTGAGGGCAG 180 GGCTTCCTCC CTACCTGATA CATTCCTGGC CAGCAGCTGC TTCCTAGCCC AGAAGCCCAG 240 TTGAGACTGT TGGACATGCT GTGTGACCTT GTGTGATGCT CTCAGCCTCT CTGGGTACTA 300 GGGCCTTTCA CCAAGACAGC CAACATGCTA AGACATGCTA TGCAGCCTCA GCATTGCCCT 360 CCCACTCTTG GCCTGTCTCC CCAGTAATAG GGTTGGTCTG GTCGTTTATC TCTATGGGTC 420 TTTCTAATGA GGAAATAGCA GAAGTAAAGG GCCAACTCAG CCCAGGCCCC ATCCACCCAT 480 GATTCATCTT AGGGTCGCCT GACCAGGAGG GTGGGGTGCC TGCTAGTGAA CCAAGAAGAG 540 AACCAGAGGG CCTGAGCAGC AAGGACCCCA CTCCTGCACT CCAAAGGGTG CAGCTGGAGA 600 GACAGGCCAG CATGGGTCGG AGAGCTCAGG CCCGGGTCAA ATCCCAGCCA CTTACCAACT 660 GCGTGGTCTT CAGCAAGTCA CTTGACCTTG CTAGGCCTCC AGCCAAAGGA ACTTCCCCAG 720 CTCTGATACG TTATTAAGAG GGAAACTTGG CCACGCACAG TGGCTCACAC CTATAATCCC 780 AGCAGTTTGG AATGCCACAG TGGGCGGATT GCTCGAGCCC AGGAATTTGA GACCAGCCTG 840 GGGAACATGG CGAAACACCA TCTCTACCAA GAACATACAA AAAATTACCC AGGCGTGATG 900 GCGCACGCCT GTGGTCCCAG CTACTCGGGA AGTTGAGGTG GGAGGATGGC TTAAGCCTGG 960 GAGGCAGAGG TTGCAGTGAG CCAAGATTGG CACCACTGTA CTCCAGTTTG AGCAACACAG 1020 CCAGACCCCG CCTCAAAAAA ATAAAAATTA GCCATGTGCG GTGGCTCACG CCTGTAATCT 1080 CAGCACTTTG GGAGGCCAAG GCAGGCAGAT CATTTAAGGT CAGGAGTTCA AGACCAGCCT 1140 CGCCAACATG GCGAAACCCT GTCTATACTA AAAATACAAA AAGTTGGGCG TGGTGGTGTG 1200 CACCTGTAAT CCCAGCTCCT CAGGAGGCTG AGGTAGGAGA ATCACTTGAA CCTGGGAGGT 1260 GGAGGTTTCA GTGAGCTGAG ATCGGGTCAT TGCACTCCAT CCTGAGAGAC AGCGAGACTC 1320 CATCTCAAAA AATAAATAAA AATAAAAATT AAAATTTTTT TTTTGAGATG GAGTCACCTA 1380 GGCTGGAGTG CAATGGCACG ATCTCGGCTC ACTGCAACCT CTGCCTCCCA GGTTGAAGCG 1440 ATTCTCCTGC CTCACTGTCT CAGCCTCCCG AGTAGCTGGG ATTACAGGTG CGCGCCACCA 1500 TGCCTGGCTA ATTGTATTTT TAGTAGAGAC GGGATTTCTC CATGTTAGCC AAGCTGATCT 1560 CAAACTCCTG ACCTCAGGTG ACCCGCCCAC CTCAGCCTCC CAAAGTACTG GGATTATAGG 1620 CATGAGCCAC CCCGCCTGGC TCAAAAATTA AAATTTTTTT TTTTGAGATG GAGTCTCACT 1680 CTTTTGCCCA AGCTGGAGTG CACAGGCACG ATCTCGGCTC ACTGCAACCT CCACCTCCCG 1740 GGTTCAAGCA ATTCTCCCTG CCTCAGCCTC CCGAGTAGCT GGGATTACAG GCGCCCGCCA 1800 CAACACCCAG CTAATTTTTG TATTTTTTAG TGGAGACGGT TTTGCCATGT TGGCCAGGCT 1860 GGTTTTGAAC TCCTGACCTC AGGTGATCCA CCCGTCTCAG CCTCCCAAAG TGCTGGGATT 1920 ACAGGTGTGA GCCACCACGC CCCGCCTAAA AATTTTTTTA AAAGAGGGAT ACCCAAGTTC 1980 AGACAGGTGA AGTGCCTCAT GATCCAGAGT CCCTGGTTCC CAGGGAGCCT GTCTGGCCTT 2040 CTGTTTCTGC CACCACATGG CCCAGAGAGG CTGGGTGCTG GCTGAGAGTT GGCTGGGGTG 2100 CCCCCCTTCC CCTATCCACC CAGACAGAAG TACTGGTGGG 2140
|
| |
|
|
|