| Tag | Content |
|---|
EnhancerAtlas ID | HS105-38382 | Organism | Homo sapiens | Tissue/cell | IMR90 | Coordinate | chr19:2315710-2316880 | 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: 2 | Chromosome | Start | End |
| chr19 | 2315855 | 2316044 | | chr19 | 2316516 | 2316762 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH19I002315 | chr19 | 2315520 | 2317161 |
| Enhancer Sequence | GGCCTGGGAA CAATTCTGAA GGTAGAATTG TCAGCATTTG CTGATGGCTG GGATGTGGGA 60
GGCAAGAGAA ACAGCAGGGA AGGGCACCCG AGGGTGTAAG CCTGAATCAT GGAGCTGTTT 120
CCTTGGATGC AGAAAGCTGG AGCGGCACCT GGTGGAAGGA GCATTGGTTT GGGGTGTGCA 180
TTAATTTTGG GGCGCCTCTG GTGCTGGGGC AGAGATGAGG TCAGGGAAAT GGAAGTCAGA 240
AGCATTTTCA ACAATGAAAG CGGAACCCAC GGGCATCTCT GTCTCTGACT TCGTGCCCAT 300
TACCCCCAGC TTCCTGTTCC CTTACTGCTT CTGGTCTGTG TTCACTGGCC GGCGTGCAGA 360
ACTCTGTCTT CTGTCGGGCA CTGGAACCCT AGCGGCCTCG GGCCCGTCAT TCCTGGGTGA 420
ATCCTGACCC CTGCTGGCTC TGGTCAGCAC GGTCGAGGCC AGCGTGGCCA CGCAGTGGCG 480
GTGGGGGGCG GGGGTCCACG GAGCTGAGTC CTGAAGGGAG GTAGAGAGTG TGAGACACTG 540
GAGGCAGAAG GGCCCGGAGT TCATAGACAG ACCTAGGCCT GCCCGGAAAG CCCCTGTCTA 600
ATGGGCAAGG CGGAGGAGCC CGGACTTATT CCTGTGGACA ATGGGGGCTT TGGGGAGGCG 660
CAGAGTGGGA GGGACCTGGT GAGATCCCAG GAGCTTGAGC CCTAGCCGTG GAGCTGGGAC 720
CCCCAGGACT GTCCTTTTTA TTTTAAGACA GGGTCTCGCT CTGTCACCCA AGCTGCAGTG 780
AGGTGGCGGA ATCATAGATC ACTGCAGCCT TGGCCTCCTA GGCTCAAGAG ATCCTCCCAC 840
CTCCTCCTCC CTAAGTGCTG GGATTACAAG TGTGAGCCAC AGTGCCTGGC CCCAGGGGTG 900
TGCTAACCTC TCTCACCCTG GGCGGTCCCC AGGCTCAAAC CAACAATTCC TGAACCCTAG 960
GAGCTCTCCT CGTGGGCACA GCTTCTTCTG TTTACAAACC TTCTTCCCTT CATATCCATG 1020
TCCTTGTCTG GGTCCAGGCA GGAAATCGAC ACCCAGAAAC AGGCGGTGAT GGGCAGCAGG 1080
GGCCTCTGTG GCAGAAGGTC TCACGCTACA CGGTACTGTC CGGGTCCTTG CACGGGTGTT 1140
CTGGAGGTGC AGGGAGGCCT CCCCTCGGTC 1170
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