Tag | Content |
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EnhancerAtlas ID | HS183-06967 | Organism | Homo sapiens | Tissue/cell | T47D-MTVL | Coordinate | chr5:179106260-179107870 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr5:179106938-179106949 | CATGAGTCACT | - | 6.14 | HNF4G | MA0484.1 | chr5:179107625-179107640 | GAAGTCCAAAGTCCA | + | 7.07 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GCGCTGCTGG GAGACAAGAG TCCGGGTGAG CAGCGTGCTT GGTACAGGCC GCCTCTCAAA 60 CCGCGAGGCC GGCGGACATG TCTTAGCCCT GCAGCTACGG CTGCGGCTGT GTCTCACCAG 120 CTGCTGGCCA CCGAGGAGCC CGTCGTTCCA CGCTGCACAG GCAGCAGTCT CACCTAAACC 180 ATCTTCCCCA AAGACCACTG AGGATCAGGC CCTGGGATAC ATATGCAGAT GAAGGACGGG 240 AGGAGGGCCT TGTTCTGAGT TGCAGCTGGA AGGGTGAGGG GTAGGGAATG GTAGCAAGAC 300 AAGTAAGTAG GTACTTAAAG GAGGAGTAGG ACTTTGCCAG GTGGGTTGAG GATGGAAAAT 360 GGAGAACTTC TAGGCAGAGG GAAGAGCCGA GCAGGGCTTT CTTTTTCTTT TTTTTTGAGA 420 CTGAGTCTCG CTGTCGTTGC CCGAGCTGGA GTGCAATTGC GCGATCTTGG CTCACTGCAA 480 CCTCCACCTC CCGGGTTCCA GCAGTTCTCC TGCCTCAGCC TCTTGAGTAG CTGAGATTAC 540 AGGCGCCTGC CATCACCCCC ACCTGATTTT TGTATTTTTA GTGAAGACGG GGTTTCACCA 600 TGTTGGCCAG GCTGGTCTCG AACTCCTGAC CTCAGGTGAT CCACCCAACT CGGCCTCCCA 660 AAGTGCCCGG ATTACAGGCA TGAGTCACTG CGCCTGGCCT TTTTTTTTTT TTTTTTTTTT 720 TTTTTGTATT TTTAGTAGAA ATGGGGTTTC ACCTTATTGG CCAGGCTGGT CTCGAACTCC 780 GGACCTCAGG TGATCTGCCC GCCTCAGCGC CAAAGTGCTG GGATTACAGG TGTGAGCCAC 840 TGTACCCGGC AGGGCAGGAC TTTCATATTT CAGATGTGAA CACGAGCTTG GATAGGATTG 900 GTGCTGGGAA GAGCAGAAGA GGAAGCTGGG AAGGTGGACC AGTGCACTAT GTGAAGGTGC 960 CCTACAGGCA GGCTCGGAAG CTTAGACTTC CTTTTGTGGG TAAGAGGGAA CTGCTGAAGG 1020 ATTAGAAAGC CGGGGTTAGA TCTGGATTCT GAAAGCAATC TGGGAGGATA TCTAGCATAG 1080 CCAACAGCAT TATTGCCCTC ATCATTCAGT CATTTGATAG ACTTGAACTA GCATCTGCTC 1140 TGTGCCAGAC TCTGGTCTTG GGAAGGGGAC CTGAAACAGC CTCTGCCTGC CCTCAAGGTG 1200 CTCCTAATCC AGCTTGGAAG ACAGATGCGT GTATAGACCA CAGTCCAGTG TGTTCACTGA 1260 CATCCTGGGG TGTGTGCCAT GGGCTAGACC TATGCATAGG GCTCAAAGTA TCAGGGATTG 1320 TGCACACTAA ACATGACTTT TATTCCAAAC AAACTGTGCC CTCAGGAAGT CCAAAGTCCA 1380 GATAACAGAC AAGTCCCATT TTGCTCACTT CTCTCTGCAC CCCCCACCCC TGCCCAGTAA 1440 GTGCTGATTC TATTATGTGA AAAAGGGAGC TATGTGTTGT TTCTAATTCC TCTTCTGCCC 1500 ATGGGCAGTG AGAAGAGAAA GAACTAGAGC AGGGTTCCCT CTGTTATGCC TTCGTTAATT 1560 CATAATACAC TTATCCCTCA CATATAGGTG GACAGAGGCT GGATGGTACA 1610
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