| Tag | Content |
|---|
EnhancerAtlas ID | HS047-00087 | Organism | Homo sapiens | Tissue/cell | Fetal_placenta | Coordinate | chr1:3597060-3598300 | 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 | TTGGATCTAA GGGAATTTCT TTCCTCCGAG TCCAGCCCCT CCAGTGCTCC TGCCCTTCAG 60
GAAACATGCC TGGGACCCCT CACTTGTGCC CACCCAGCCT TGGCCCACAT ACCTGCACCA 120
AGAGGCTACC CTACTCATAC TGCTCAGCCC AAAGGGACCC ACCGTGGGGT ATGGGCAAGG 180
GCGGGTTCTG CTCTCCCCCG GGGCCCTGTG CCAGCCTCAG CTGGACCTGC GGTTCTGCTT 240
CCTGTCACAC TCTCCCATTT TAAATTAACG GAATGGTGCG GTCCCCATGC ACACCCTCAG 300
CTCCACTGGG GTTTTAGCCC AGCCCAGGAT CGGAGGCCTG CAAGGGCACA CCCACCTGGC 360
CACGTGATGG TGAAGTGGGG TGGGGCAGGG CAACCAAATT AACTTCTAAT TCTAAGAGCC 420
CCTGGAGCAT TCATCACCAG CACTTACAGC CGTGTGACCT CACACAAGTC ACTTAACCCC 480
TCTGAGCCTT GGGGCTCCTG AAAAGTGGAT GGAGCGGTCA CGCCCACCTG GGAGAGGTGG 540
CTTGGGCCAG CACCCTCTAA GCTGCTTGTC CCAGGCCATC ATGGCTCACG GACCGCCCCT 600
CAGCCTGGCC TGTGCCACTT CTCCAGGGCC CGGCACGTGG CAGCCACAGG CTTCTATCAG 660
CTCCCGCCTG CCTGGGGAAG GACAAAAACG ACAGGTTCCA GGCCATGGCC TGCACCCCCG 720
CTGGCCGTGG GCAGGTCCAG GCCTGCCTGC CTGAGCATTG CAGGGCGGTG GCCAAGCCTG 780
TCCCATAGCA CCTCACCGAG GACCTGGGAG GCTGGCCCAG GGGAGAGGTC ACCTCAGCCG 840
GGGCTGGGGG CTGTGGGCAG GGTGGGCTCG GGTTTCCCTG TCCCCTCCCC CAGCTGTGCT 900
CTGCCTGGAC ACTGCCACCT CCTCATGGGT GTCCAGGGCC ACTGGGAGCT GGGCCCAGGG 960
GTTCTCAGGG GAGCAATGGT GGAGACAAAG ACCAGCGGAC GGGCGCTGGG GTCAGAGCTC 1020
TCCAATCCCT GGGTGTCTCC TTCTCAAGGC GTGACCACCC AGGCAGTGGC CGGCTGCAGG 1080
ACAGGGCAGC TTCAAGTTCC CAGCCTTGCC AGGCTTCCCT GTGGCCCTGG GGTGCAGGAA 1140
GGAGCCCCAG CTCAGAAGGC GAGGGGGCGT CTGTGTCCTG CAGCAGTGGG CACAGCTAGG 1200
CTCTAGCCGG GGGCTTGGCT GCAGCCTCCA GCGCAGCCCT 1240
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