Tag | Content |
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EnhancerAtlas ID | HS095-00101 | Organism | Homo sapiens | Tissue/cell | HMEC | Coordinate | chr1:3597150-3598410 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF14 | MA0740.1 | chr1:3597575-3597589 | GGTCACGCCCACCT | + | 6.43 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CACCCAGCCT TGGCCCACAT ACCTGCACCA AGAGGCTACC CTACTCATAC TGCTCAGCCC 60 AAAGGGACCC ACCGTGGGGT ATGGGCAAGG GCGGGTTCTG CTCTCCCCCG GGGCCCTGTG 120 CCAGCCTCAG CTGGACCTGC GGTTCTGCTT CCTGTCACAC TCTCCCATTT TAAATTAACG 180 GAATGGTGCG GTCCCCATGC ACACCCTCAG CTCCACTGGG GTTTTAGCCC AGCCCAGGAT 240 CGGAGGCCTG CAAGGGCACA CCCACCTGGC CACGTGATGG TGAAGTGGGG TGGGGCAGGG 300 CAACCAAATT AACTTCTAAT TCTAAGAGCC CCTGGAGCAT TCATCACCAG CACTTACAGC 360 CGTGTGACCT CACACAAGTC ACTTAACCCC TCTGAGCCTT GGGGCTCCTG AAAAGTGGAT 420 GGAGCGGTCA CGCCCACCTG GGAGAGGTGG CTTGGGCCAG CACCCTCTAA GCTGCTTGTC 480 CCAGGCCATC ATGGCTCACG GACCGCCCCT CAGCCTGGCC TGTGCCACTT CTCCAGGGCC 540 CGGCACGTGG CAGCCACAGG CTTCTATCAG CTCCCGCCTG CCTGGGGAAG GACAAAAACG 600 ACAGGTTCCA GGCCATGGCC TGCACCCCCG CTGGCCGTGG GCAGGTCCAG GCCTGCCTGC 660 CTGAGCATTG CAGGGCGGTG GCCAAGCCTG TCCCATAGCA CCTCACCGAG GACCTGGGAG 720 GCTGGCCCAG GGGAGAGGTC ACCTCAGCCG GGGCTGGGGG CTGTGGGCAG GGTGGGCTCG 780 GGTTTCCCTG TCCCCTCCCC CAGCTGTGCT CTGCCTGGAC ACTGCCACCT CCTCATGGGT 840 GTCCAGGGCC ACTGGGAGCT GGGCCCAGGG GTTCTCAGGG GAGCAATGGT GGAGACAAAG 900 ACCAGCGGAC GGGCGCTGGG GTCAGAGCTC TCCAATCCCT GGGTGTCTCC TTCTCAAGGC 960 GTGACCACCC AGGCAGTGGC CGGCTGCAGG ACAGGGCAGC TTCAAGTTCC CAGCCTTGCC 1020 AGGCTTCCCT GTGGCCCTGG GGTGCAGGAA GGAGCCCCAG CTCAGAAGGC GAGGGGGCGT 1080 CTGTGTCCTG CAGCAGTGGG CACAGCTAGG CTCTAGCCGG GGGCTTGGCT GCAGCCTCCA 1140 GCGCAGCCCT CACACACGCT GTTCCCAAGA TGGGGTGACC GGGACCGGAG CCACCTCCAG 1200 GTCCCGGGCA TCAGGGAGAC CCCAAACCTG GCTGCATCCC CCAGGCCAAA CCCAGACACA 1260
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