| Tag | Content |
|---|
EnhancerAtlas ID | HS047-17338 | Organism | Homo sapiens | Tissue/cell | Fetal_placenta | Coordinate | chr19:33901190-33902290 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TFAP2C | MA0524.2 | chr19:33901882-33901894 | TGCCCCGGGGCA | + | 6.74 | | TFAP2C | MA0524.2 | chr19:33901882-33901894 | TGCCCCGGGGCA | - | 6.74 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AGCTCATCAG CTATGGACCT GGGTGAGCGG GGAGCCCGGG CAGTCTCAGT AGGCCATGTG 60
CCCAAGGGCA GGGAGGACCC CGAGACTGAG TGTGTTCCTG CAAATACTCG GCCCTGACAG 120
CTCAACGCTC GGCAGCTCTC TGGGCAGCTG GTTGTCTGTC CATAGGTCTG GGCATGTGTG 180
TTCCTGTCCT TCAGTGGGCA TGGCTGGGGA CTCTGGGGGG TGGGCTCCCA CGACTACCTG 240
CTGTAGGGTG AGGCGGGGTC CAGGCCGGTG AGCAGCCATC ATGGGAACTC CCGCTGGAGG 300
AGCTGGCACA TTGGGGTGGC TCCTCGATGG GAAGGCGGAG GCAGCCCAGC TGGGCGCCAC 360
GCAGGCCTCA GAGGACATGC CATGCTGCTG GGGGGCAGAG GGCTCTGCAG GAGGCTTGTT 420
CGGGTGCATC TGCCATAGAA GAAAGGGCAC CAAAGAACTG GGAGGGACAA GGCACATCCT 480
CTGCTAGTCA GTGACCACAG TGAAATGTCT GGAGGCCAAG ACAGGGCCTG CGTGGCTGTG 540
GCTGAGCCCC AGGGCTCCAG CACTGGGGTA GCTCTCAGGA GCTCTGCACT GCCTGGGCTG 600
GCCCTGGCTG ACATCTGACG TGCAGGGCAC AGGCAAAGAA CGCGGAGGGA CTGAGCAGAG 660
GCCAGGCTGC AAGTACTCAC ACACCTCCTC CCTGCCCCGG GGCAGCGGCC CAGCTGCTCT 720
GCCCTGCACA CCGAGGGGCT GTGGGTAGGA CTGCAAGTCC TCCAATGAGA GAAAAGACTA 780
CCCGAGGGGC GGAGGCCGCA GGGCCTGCCC ACATCTCCTT GTCGTGGCTT CTATGAAGAA 840
CTGTGAGCAC GGCACATCGT GCTCAGGAAA GCCCTGCACG CAGCCACGGG TCAGCACTGC 900
TGACTTGCTG AACGCAGGGC CGCAGAGGCC ACGGGCTCCT GCAGCAGGAG GATGGCAGGT 960
TTCAGAGCGT GGGAGGCTCC CTGCGGTCTT CCCAGCTCCA GACCAAGAGG CCTGCCCTCC 1020
TGGCACCAAG ACAGAAAGAT GCGAGCGTGG TGCCCCCTGA ACGGAGAGGA CAGCCTGGAC 1080
AGAGGCTGGG GATGGTTCAG 1100
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