| Tag | Content |
|---|
EnhancerAtlas ID | HS053-00077 | Organism | Homo sapiens | Tissue/cell | Foreskin_keratinocyte | Coordinate | chr1:3597100-3598390 | 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 | CCAGTGCTCC TGCCCTTCAG GAAACATGCC TGGGACCCCT CACTTGTGCC CACCCAGCCT 60
TGGCCCACAT ACCTGCACCA AGAGGCTACC CTACTCATAC TGCTCAGCCC AAAGGGACCC 120
ACCGTGGGGT ATGGGCAAGG GCGGGTTCTG CTCTCCCCCG GGGCCCTGTG CCAGCCTCAG 180
CTGGACCTGC GGTTCTGCTT CCTGTCACAC TCTCCCATTT TAAATTAACG GAATGGTGCG 240
GTCCCCATGC ACACCCTCAG CTCCACTGGG GTTTTAGCCC AGCCCAGGAT CGGAGGCCTG 300
CAAGGGCACA CCCACCTGGC CACGTGATGG TGAAGTGGGG TGGGGCAGGG CAACCAAATT 360
AACTTCTAAT TCTAAGAGCC CCTGGAGCAT TCATCACCAG CACTTACAGC CGTGTGACCT 420
CACACAAGTC ACTTAACCCC TCTGAGCCTT GGGGCTCCTG AAAAGTGGAT GGAGCGGTCA 480
CGCCCACCTG GGAGAGGTGG CTTGGGCCAG CACCCTCTAA GCTGCTTGTC CCAGGCCATC 540
ATGGCTCACG GACCGCCCCT CAGCCTGGCC TGTGCCACTT CTCCAGGGCC CGGCACGTGG 600
CAGCCACAGG CTTCTATCAG CTCCCGCCTG CCTGGGGAAG GACAAAAACG ACAGGTTCCA 660
GGCCATGGCC TGCACCCCCG CTGGCCGTGG GCAGGTCCAG GCCTGCCTGC CTGAGCATTG 720
CAGGGCGGTG GCCAAGCCTG TCCCATAGCA CCTCACCGAG GACCTGGGAG GCTGGCCCAG 780
GGGAGAGGTC ACCTCAGCCG GGGCTGGGGG CTGTGGGCAG GGTGGGCTCG GGTTTCCCTG 840
TCCCCTCCCC CAGCTGTGCT CTGCCTGGAC ACTGCCACCT CCTCATGGGT GTCCAGGGCC 900
ACTGGGAGCT GGGCCCAGGG GTTCTCAGGG GAGCAATGGT GGAGACAAAG ACCAGCGGAC 960
GGGCGCTGGG GTCAGAGCTC TCCAATCCCT GGGTGTCTCC TTCTCAAGGC GTGACCACCC 1020
AGGCAGTGGC CGGCTGCAGG ACAGGGCAGC TTCAAGTTCC CAGCCTTGCC AGGCTTCCCT 1080
GTGGCCCTGG GGTGCAGGAA GGAGCCCCAG CTCAGAAGGC GAGGGGGCGT CTGTGTCCTG 1140
CAGCAGTGGG CACAGCTAGG CTCTAGCCGG GGGCTTGGCT GCAGCCTCCA GCGCAGCCCT 1200
CACACACGCT GTTCCCAAGA TGGGGTGACC GGGACCGGAG CCACCTCCAG GTCCCGGGCA 1260
TCAGGGAGAC CCCAAACCTG GCTGCATCCC 1290
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