| Tag | Content |
|---|
EnhancerAtlas ID | HS047-16416 | Organism | Homo sapiens | Tissue/cell | Fetal_placenta | Coordinate | chr19:2315660-2316650 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr19:2316542-2316563 | CCTCCCACCTCCTCCTCCCTA | - | 6.54 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH19I002315 | chr19 | 2315520 | 2317161 |
| Enhancer Sequence | TGCCTCGGCC TCCCAAAGCA CTGGGATTTC AGGCGTGAGC CACCGTGCCT GGCCTGGGAA 60
CAATTCTGAA GGTAGAATTG TCAGCATTTG CTGATGGCTG GGATGTGGGA GGCAAGAGAA 120
ACAGCAGGGA AGGGCACCCG AGGGTGTAAG CCTGAATCAT GGAGCTGTTT CCTTGGATGC 180
AGAAAGCTGG AGCGGCACCT GGTGGAAGGA GCATTGGTTT GGGGTGTGCA TTAATTTTGG 240
GGCGCCTCTG GTGCTGGGGC AGAGATGAGG TCAGGGAAAT GGAAGTCAGA AGCATTTTCA 300
ACAATGAAAG CGGAACCCAC GGGCATCTCT GTCTCTGACT TCGTGCCCAT TACCCCCAGC 360
TTCCTGTTCC CTTACTGCTT CTGGTCTGTG TTCACTGGCC GGCGTGCAGA ACTCTGTCTT 420
CTGTCGGGCA CTGGAACCCT AGCGGCCTCG GGCCCGTCAT TCCTGGGTGA ATCCTGACCC 480
CTGCTGGCTC TGGTCAGCAC GGTCGAGGCC AGCGTGGCCA CGCAGTGGCG GTGGGGGGCG 540
GGGGTCCACG GAGCTGAGTC CTGAAGGGAG GTAGAGAGTG TGAGACACTG GAGGCAGAAG 600
GGCCCGGAGT TCATAGACAG ACCTAGGCCT GCCCGGAAAG CCCCTGTCTA ATGGGCAAGG 660
CGGAGGAGCC CGGACTTATT CCTGTGGACA ATGGGGGCTT TGGGGAGGCG CAGAGTGGGA 720
GGGACCTGGT GAGATCCCAG GAGCTTGAGC CCTAGCCGTG GAGCTGGGAC CCCCAGGACT 780
GTCCTTTTTA TTTTAAGACA GGGTCTCGCT CTGTCACCCA AGCTGCAGTG AGGTGGCGGA 840
ATCATAGATC ACTGCAGCCT TGGCCTCCTA GGCTCAAGAG ATCCTCCCAC CTCCTCCTCC 900
CTAAGTGCTG GGATTACAAG TGTGAGCCAC AGTGCCTGGC CCCAGGGGTG TGCTAACCTC 960
TCTCACCCTG GGCGGTCCCC AGGCTCAAAC 990
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