| Tag | Content |
|---|
EnhancerAtlas ID | HS040-00161 | Organism | Homo sapiens | Tissue/cell | Esophagus | Coordinate | chr1:3597110-3598250 | 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 | TGCCCTTCAG GAAACATGCC TGGGACCCCT CACTTGTGCC CACCCAGCCT TGGCCCACAT 60
ACCTGCACCA AGAGGCTACC CTACTCATAC TGCTCAGCCC AAAGGGACCC ACCGTGGGGT 120
ATGGGCAAGG GCGGGTTCTG CTCTCCCCCG GGGCCCTGTG CCAGCCTCAG CTGGACCTGC 180
GGTTCTGCTT CCTGTCACAC TCTCCCATTT TAAATTAACG GAATGGTGCG GTCCCCATGC 240
ACACCCTCAG CTCCACTGGG GTTTTAGCCC AGCCCAGGAT CGGAGGCCTG CAAGGGCACA 300
CCCACCTGGC CACGTGATGG TGAAGTGGGG TGGGGCAGGG CAACCAAATT AACTTCTAAT 360
TCTAAGAGCC CCTGGAGCAT TCATCACCAG CACTTACAGC CGTGTGACCT CACACAAGTC 420
ACTTAACCCC TCTGAGCCTT GGGGCTCCTG AAAAGTGGAT GGAGCGGTCA CGCCCACCTG 480
GGAGAGGTGG CTTGGGCCAG CACCCTCTAA GCTGCTTGTC CCAGGCCATC ATGGCTCACG 540
GACCGCCCCT CAGCCTGGCC TGTGCCACTT CTCCAGGGCC CGGCACGTGG CAGCCACAGG 600
CTTCTATCAG CTCCCGCCTG CCTGGGGAAG GACAAAAACG ACAGGTTCCA GGCCATGGCC 660
TGCACCCCCG CTGGCCGTGG GCAGGTCCAG GCCTGCCTGC CTGAGCATTG CAGGGCGGTG 720
GCCAAGCCTG TCCCATAGCA CCTCACCGAG GACCTGGGAG GCTGGCCCAG GGGAGAGGTC 780
ACCTCAGCCG GGGCTGGGGG CTGTGGGCAG GGTGGGCTCG GGTTTCCCTG TCCCCTCCCC 840
CAGCTGTGCT CTGCCTGGAC ACTGCCACCT CCTCATGGGT GTCCAGGGCC ACTGGGAGCT 900
GGGCCCAGGG GTTCTCAGGG GAGCAATGGT GGAGACAAAG ACCAGCGGAC GGGCGCTGGG 960
GTCAGAGCTC TCCAATCCCT GGGTGTCTCC TTCTCAAGGC GTGACCACCC AGGCAGTGGC 1020
CGGCTGCAGG ACAGGGCAGC TTCAAGTTCC CAGCCTTGCC AGGCTTCCCT GTGGCCCTGG 1080
GGTGCAGGAA GGAGCCCCAG CTCAGAAGGC GAGGGGGCGT CTGTGTCCTG CAGCAGTGGG 1140
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