| Tag | Content |
|---|
EnhancerAtlas ID | HS043-15770 | Organism | Homo sapiens | Tissue/cell | Fetal_heart | Coordinate | chr16:2184430-2185470 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF16 | MA0741.1 | chr16:2185222-2185233 | GCCCCGCCCCC | + | 6.02 | | KLF5 | MA0599.1 | chr16:2185222-2185232 | GCCCCGCCCC | + | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CAAGGAGACA CTGTCCCGGC GAGGAGCCTG GAGCCTGGGA AATACAAGGC ATCAGACTGG 60
TCCCAAGACT CTCCCCAGCG CTGGGGACAA CTGTCTGCTT ATCTTAGTCC CCTCCGCCCT 120
TTTCAATCCA ACCCTGGGTC CTGGGCACCT CATAGTTCCA AACCCCTGCT ATGCACATCC 180
CGGCTGTGAT GCCTGGGACA GGTCGTGTCA CCTCTCCAAA CCTGTTTCCT CATCTGTGAA 240
ATGCAAATCT CCACGGTCCC TATGCCTCGG ATGGTCAGAG TCAGGATTCC GCATGACGAC 300
CCCCAACAGG AGCCTGGCAC AGACCTGGCT CTGGGCAGCG TCTCCATAAA GGCCACCTGT 360
TGTTTTTATC TCCCGAAAGC GAACATGACA AGGCTTTAAC CCCCCACGGC AATCCCCCCT 420
CACCCCTGTT CTCAGGATAG CCTTGGAACC CAATAGCAGA GCGCCTGAGG CCCTTCATGA 480
CCCCAGCCCA CCCGCGAGCC CACCTCCCAC CCTGCCCCTA CCCCTCACAC CTCCCGTGGC 540
CAGCCTCCAG CCTCACGGTC TTTGCTCACA CCGTTCACCC CCCTTCTTCT GGACCCACCT 600
CATCGCCCCT TCCTAAGCAT CAGCCCAATT CTTGCACATC CATCAAATCC TTTTCCAGAC 660
ACCTCCTGGA ACTCTTCCCT GCCGCCCCCT ACAGCCATCC CCACCTCTCC GGGTACCCCG 720
CAGCCCCAGG CCGCATCCCA ATTCCTCTCC AATTAGCGAC TGTTTGTCCT CCCAGCTGAG 780
CGCGGCCTCC GCGCCCCGCC CCCGCTGGCG TCTGCAGAGC CCCCGGGTGG GACGTCTGTC 840
TCCAGACCCG GGGTTTTTCG GCTCCCCGGG GCCGTGCCAA CCGCGGCTCC AGGCGTTCCT 900
TATTTAGCAG GGCCGCCGTG CCGCGCCGGA GCCTCGCCCT GGGAGCGTCC TGGCCCGCGT 960
CCTGCTTCCC GTCCCGGGCC AGGGAACGCG CCCACGCCCG CCCGTCCCGC GGCCTCTCCC 1020
GGGTGCCGCT GGGCCCGCTA 1040
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