Tag | Content |
---|
EnhancerAtlas ID | HS091-24813 | Organism | Homo sapiens | Tissue/cell | HepG2 | Coordinate | chr19:57914320-57917220 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFYB | MA0502.1 | chr19:57914727-57914742 | CCATGGACCAATCAG | + | 6.98 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GTGTGTAGCA TTTTAGTCAC ATTAAAATGC AGTTATGGCA GCATGCTGTG TTCTCTATCT 60 GAAGAATTCA CTAGTCACTT GAACACTTTG GAGTCCTCAC CCCCCTCCTA TGATTGATTA 120 GGGCATAGAC ATCAGCCTTG GACAGAAGAC ATGGACTGGC TTTGGCAGGC AGATTGCAGA 180 AATTTCCTTT CTCCAGGGGA AAGTATTGGT TATCTCATTG ATAGTGGTAG GAGGCAGATA 240 CATTGCTAGG CAGACTAAGG ACGGGTCCCT GGTGAAACCC AAACTTCAAG CCAACGACAG 300 TTTAAAGCCT GAAAATTGAG CTGCCAGTTC CAAGTAGAGT CCATGACTGG AGTGAGAACT 360 TCCTCAATGC CTTTTAGCCA ATCAAATGGT GCTTTTTCCA GGCCCACCCA TGGACCAATC 420 AGTATGCAGT CTCCATTCTG AGCCCATAAA AACCCTGGGC CCAGCTACAC ATTGGGCTAC 480 CCACTTTCAG GTCCCCTCTT GTTGAGAGCT TTTCTGCCAC TCAATAAAGT TCCCTGCCTT 540 GCTCACTCTC TGGTGTCCAC ATAACATCAT TCTTCTTGGT CATGGGACAA GAACTCGGAA 600 ACTGCCAAAT GGCGGGTGTG AAAGGAGCTG TAACACTGTA GCCCTCCTGC CTTCCACCAG 660 CCCCAGGCAG CCACCCCATG TGACAGGAAG CAGCGGCAGC AGGGCCAGGC CAGCCCATGA 720 GCCATGGGCT GGAGCAGGGT GGCAGGACCA AACAAGCTGT GACACACCCC CATTCACTGA 780 AGTGTGTGGA TGGTGGGAAC AGACAAGCTG TAACACAAAT GAGCTGTAAT GCTTCCTTGG 840 GGCTCAGACC TTGGGATTCC CTGAGCAAAA GCTGTAACAC CCCTTGGGGC TCTGTGGTTG 900 CTGGCGTCTC TGAGTTTTTG GGCGCTGCCA TGTCCCCCTT GTCCAGATAC CAGCTTCCAA 960 GGCAGAAGCC GGTCGCAGCA CGCCTGGACC AGCTGTAGGC CAAGCACAGA GCCATGGTGG 1020 GCACAGGATC CGGCTGGTAA CATGAGCCAA GCACAGCCTG TCGGACTGAG TTAGTTGAGT 1080 GAGTCCAGCA GGCCAAGTGA TGTCTGGGCA GAAGTGCTTC AGCCATGGAG GTTTCTGCCT 1140 GGTGAAGTGG CACTGAAAGT ATCTTGTGTC ATCATGACAC TTGGGATGGA ATTTTCCAAC 1200 CTGCCAGTCA CCCACACTGT GAACTCCTTC TCACCCCTAA TGCACACACA TACCCTGGTT 1260 GGTTTTGTGA TAATAAAGGT CACATTGTTT AAGCTACCTT AACTCTTGGA AATCTAGTCA 1320 CCGTATGCAG TGGGTTTTGA ACAGAATTGG TCTCTGCTAG AATAAAAGCA TGAATGGTTT 1380 TTTGTGGGAC CTTTACTTTG TGAGCTCCAG AGGGACTAGT AGGAAGCAAA AGATCAGCTC 1440 GTATGCAGAT TTGGGCCAAT TTGCATTGCC ATGAGAAGCC TCCTGGGAAA GTCTGAAGGA 1500 CTTCTGCACA AAATTTCAAG CCCTGAGTAC AAAGATTATT TGTATTCAGA AAAGTACAAT 1560 TTGAGGAGAA AACAGTTGCC TTGATGTTTA AGGCATTGGG CAACAGTATG CATTGGGTAT 1620 CCCTACCCAT ATTTCCCATA TTTCCCCTGC ATTGATGAGG GATAGCTGTT TCTTGTGACC 1680 TGCTGGAAGC TATGGGTCCT GAAGTAAAAC ACTATCTAGG TATATGTTCC TGGCTGTTGA 1740 CCTTTAGGGC TAGATGGAAG CCATATTCTT TTTTTTTTTT TTTTTTCTTG AGACGTAGTC 1800 TCGCTCTGTT GCCCAGGCTG GAGTGCAGTG GGATGATCTC AGCTCACTGC AACCTCGCTT 1860 CCTGGGTTCA AACAATTATC CTGCCTCAGC CTTCCGAGTA GCTGGGACTA TAGGTGCACG 1920 CCACCACACC CGGCTAATTT TTGTATTTTT ATTAGAGATG GGGTTTCACC ATATTATATT 1980 GGCCAGGCTA GTCTCAAACT CCTGACCTCG TGATCCGCCC ACCTCAGCCT CCCAAAGTGC 2040 CAGGATTACA GGAGTGAGCC ACTGCACCTG GCCAGAAGCC ATATTCTATA ATAAATAGTG 2100 GTTGGATTAA TAGGACATGG GAGAGACTGC AGTAGAGTGG ATGAGTCCCC TCTAAAGGAG 2160 CACTCACAAA TGCCCTGGTA GCTATGGCTG TGTGGGGTGG GGTATTACAG GAATTCCAAA 2220 GACCTAAGGA GCTGTGTACC TCCTGTAGCC AAGGTCAATG TCAGAACAAC TAAATCAATG 2280 ATTTTATGAA TTCCTGTAGC CTCCCTGGAC TATAAATTTC AAACCATAGT TGCATCATCT 2340 ACATAGTGAT GGGCCTTGAG CCTTCCCTAA AGATAAAAAG CCTACATAGC CCGTGCTGCC 2400 CCATCACCTG TGTGTCGGAA CATCTTCCTT GTTTCAAGCT ACATGAGTGC TTTTTTATTC 2460 TGTTGAAGTG TGTCATGTCA TGCCTGGTGA ATTAATAAAT CTGTCCTCTG CAACTGACAG 2520 GGTTCTTCCA CTGTGAAACA AGAGGGTTGT ATATAGGTTG CGTTTAACTA ACAGAGTTAA 2580 TTAAACCTTT TTACTTTAAA AATTACTCAG TCTTGGGCCA GGCGCGGTGG CTCACGCCTG 2640 TAATCCCAGC ACTTTGGGAG GCCGAGGCAG GCGGATCACG ATGTCAGGAG ATCGAGACCA 2700 TCCTGGCTAA CACAGTGAAA CCCCGTCTCT ACTAAAAATA CAAAAATTAG CTGGGCGTGG 2760 TGGCAGGCAC CTGTAATCCC AGCTACTCAG GAGGCTGAGG CAGGAGAATC ACTTGAGCCC 2820 AGGAGTTGGA GATTGTGGCG AGCCGAGATT GCGCCATTGC ACTACAGCCT GGGCAACAAG 2880 AGTGAAACTC CATCTTTTTT 2900
|
| |
|
|
|