Tag | Content |
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EnhancerAtlas ID | HS102-07499 | Organism | Homo sapiens | Tissue/cell | HuCCT1 | Coordinate | chr14:75378540-75379940 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
E2F6 | MA0471.1 | chr14:75379647-75379658 | GGGCGGGAAGG | + | 6.62 | RARA(var.2) | MA0730.1 | chr14:75378598-75378615 | TGACCCCAGCCTGACCC | - | 6.38 | YY1 | MA0095.2 | chr14:75379311-75379323 | GCAGCCATGTTG | - | 6.14 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GCACCTGCCA AAGTCCAAGA GGCACTGGTT AAGGCAGGTA CTAGCTCCTG GGGCTCCGTG 60 ACCCCAGCCT GACCCCCTCC CAGGTTCCTC CACTGAGGCT GACTCACTCC AGTGGCAGGG 120 CAGGGAGGGC GGGCTTTGGT GGCACTCCTG AAGCAGACAT CGATCCTATC CTGCTCACCC 180 ACCCCTGCTA GACCTGTGGT CTCAGATGCT GCCTCCTCCA GGAAGCCTTC CCAAGATTAC 240 AGGGGCTGGG GTCCCTAATC TGCCTCCAAT GCTCTCTTAG TTCACCCTTA GGAGAGCCTC 300 TTCACACTGT CTAATCTGTC TCCCACTGGA CTGTGAGCTC AGTATTCCCG GAGCCCTGCA 360 CAGTGCAGGG ATGTAGTAGG TGCTAGACAC ATGCACTGTG AGCAGCCCGG GCCTTGGCTC 420 ACTGTGTGCG TGGTGGGCAT GCGAGCAGAA TGCCCTGCCC TCTCCCTGCC CACGCTGGGC 480 CAGGCCTCAT GCCACCTGAC GGGAGGGCTG AGAAGCCCTG TTCCACCTGG ACCCCAGAGA 540 TCAGCTGAGA AGCCCTGTTC CACCTGGACC CCAGAGATCA ACTGAGAAGC CCTGTTCCAA 600 CTGGACCTCC AGAGATCAAC CCCTCACCCA AGGCCTTAGC TAGAGCCCCA ACATCCTGCA 660 GGGTCTGAGG TGTCATGGCT GGAAGGGACC TCAGAGCCAG TCACTTCCTC TGATCTCTTG 720 TTTTACAACT GAGGAAGCCG CAGCTCTGAG GTGACTCCAG GTCTCCCCAG CGCAGCCATG 780 TTGTGTGGGC TTGGCACGCT GCGTTCAGGC CTTTTTCCCA CTCCACTCCA CCCCCTTCAT 840 TTACACACAC CCCCATGACA CAAGTTTATC TATGTGAAAA ACCTGCACAT GTACTCCTGA 900 CTGCAAATAA AAATTTAAAA TAAATAAGTA AAGTCCGCTT GAGAGGCCGT CTTTGGAGAG 960 CAGCCTCTCC TTCTTGTGTT GGTTTCCATT AGAGGCAGAC GCTGTCAATC GCAAGGTCAG 1020 GGCCATGTTT GGAGTTGGGC CCTTGACTCA TCTGCATGGT GGGCAGGGGC GGGCCCCAGC 1080 ATAGGAGCGG GCACATGGGT ACGTCGAGGG CGGGAAGGCA GAGGATTCAG CCCAGGTGAG 1140 GGCATGTGGA GGCAAGGCCA GCACCCTGGG GTTGTGACTC CTTGGCTGTT GGCCTGCCCT 1200 GCGGACATTC CCCAGGGAGG CTGTGGCCAG CCATGGTCGG GGTGGGAACT GGGCCCTGAG 1260 GCCAGGCTGC TGGGCAGTGA GGAAGGCCAC AGCTTGGGAT CAGGGTAGGG GAAGGGGCAC 1320 TGGGCTTCGA TCCTGGGCAA ATTGAATTGA TTTTCTCATC TACCAACCAG GAATTCCAAA 1380 TGCCTACCTT CCCTACATCT 1400
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