Tag | Content |
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EnhancerAtlas ID | HS053-04731 | Organism | Homo sapiens | Tissue/cell | Foreskin_keratinocyte | Coordinate | chr10:28591040-28592510 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF16 | MA0741.1 | chr10:28591593-28591604 | GCCCCGCCCCC | + | 6.02 | KLF5 | MA0599.1 | chr10:28591576-28591586 | GCCCCGCCCC | + | 6.02 | KLF5 | MA0599.1 | chr10:28591593-28591603 | GCCCCGCCCC | + | 6.02 | KLF5 | MA0599.1 | chr10:28592031-28592041 | GGGGCGGGGC | - | 6.02 | KLF5 | MA0599.1 | chr10:28592036-28592046 | GGGGCGGGGC | - | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TTCTACTCCC ACCCATGGCA CAGTGACAGA AACAAGGTCC CACCCCCACA ATCCTTTCAA 60 ACCTGCACAG GCATTCCTCA CGAACACTCC TCCCCCTCAT TCCTACCTCA CCGCTCCCCA 120 CTTCAGCCCA GACAAAGCTG AGTTACTCGG CTGGGTCTAC CTGTCACTTA AGAAAAAGCC 180 CCCAAATAGA TTCACGCTAA ATGCTGCTTT TAATTTTTTA AATAGCAAAT AAGTAAATAA 240 ATAATGCTAT CGTGTAGATT ACACGGCCAA ACGCCTGTTC TCAGAAAACA TGTAATTAAC 300 ACGACCCAAG TGAAGACGCC TTTCTGGCTT AGGGAAAGAA AAAAAAGAAG CCAGCCAGCT 360 TATCGCTCCC TTTCAGTCGG TTCTTTTCCC CGGGGAGCCG GACTCTGACT CAACTCCGCA 420 GTTTTTCCTC CACCTGTCGG TTCTCCCCGC TCTGGGTCTG CCCCGCCGCC GCCCCCGCCC 480 GGAGTCCCGC GCGTCAACAG GGGTCTCCAG GGGTCCTCAG GGTCCCGCCC GAGGCGGCCC 540 CGCCCCTGCC CCGGCCCCGC CCCCACCTCC TCACAAGGTG CCCGCCGCGG GCTCCCAGGC 600 TGAGGCGCCT AGAGGCCGGC AGGAGGCTCC GGAGGACCGC GGCACCGCTC GGCCCGGTCG 660 CCGGCGCAGG GAGCAGCTTC GGGGGCCGAC CCCACCGCCC GAGCCTAGCC CTGGGCTCCG 720 ACAGGCGCTC CCCAGAGGCG CCCCATTACC TGCTCTGGGC TGCCGCGGTC CGCGGGCAGG 780 AGGCGCACTC GCTCTGGCCC CTGCAGCCCC GGGCCCGGAG GCAAGGAGGC AGCGACCGCC 840 ACCGCCGCAG AGGACAATCG GGAGCCAGCG GGCTCGGCAC CGCCGCGGCG GGCGCAGAAC 900 GCACGAGCCC AGTGGGAGCC CGGCCCCCGC CTCCAGCCCG GCTAGTAACC AACACGGCCC 960 CCACCCTCGG AGGGGCGGGA CCGCGGTTGG AGGGGCGGGG CGGGGCTGCA CCGCCCGCGG 1020 GTAAGAGGGG CCTGCTGATA GGCTGCGAAG GCGATAGGCG TCTCAGACTT GAAGACGCCT 1080 CTCCAGCAGA ACTCCCTCAT TGGTCGGCAA GAGAAAACAA AGCTGGGCTC TGATTGGTGA 1140 CAGCTCTGTA GCTCCTCCTC ATACCCGCAG TCCCCGCAAG TTCCACCCCT GCCCGCCCGG 1200 TTCGCTCGCC CTTGGTTCCC ACTCCCAGGT GGCTGCAGAC TGGAGTGTGT TTCATGGACG 1260 AGCAACCTCC CTGAGGAGAA CCCCGGATAC GCAGGTTCAT TCGCCAGATG CGAGTTTTCT 1320 TAAGCCGCTG CGATTCTCTG ATTTCAGTAT GAACTTGGTG AATAACGTAA TCTTTAACTT 1380 CCTTTGGATT CAGACAAGTC TCCTAGGTTT AAAAATGCTG CATAAGATTG AGAGGGATAT 1440 TGTTATGCAC GAAAAAAGAC ATAAGGTGTT 1470
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