Tag | Content |
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EnhancerAtlas ID | HS111-02434 |
Organism | Homo sapiens |
Tissue/cell | KB |
Coordinate | chr19:572700-573840 |
Target genes | Number: 19 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Zfx | MA0146.2 | chr19:572901-572915 | CCCGGCGCGGCCTG | + | 6.1 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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Enhancer Sequence | GGTGAGGAGC GGGTAGGGGG CGGGGGTGCG GTCCTGCAGG GGCCGGGAAT GGAGGCCGCG 60 GTGCCGACCC GAAGCCGACG GGAGCCTGGG GCCTCGGCGC GGGGCGGCCT GGGGTGCGAA 120 AGGCCGGCCC CGGGGGCTTC CCGCGCCAGC ATGGAGCTTG GGGGTGAAGT CCCAGGGTTT 180 GAGGGGGGAC TAGAGGTTCC TCCCGGCGCG GCCTGCCGGG CTCCCCCGGG CGCTCCGGCC 240 TCGAGCCCGG CCTCTGTGTG TGGGCGTGAA GCTCCCTGCT TGGAGGCGGG AGCCAGGGGG 300 TCCTGGCCAG GCCGGTCTTG GTCAGGGGAG GTGGGCGTCT TGCTTTTCGG TCACCTGGGG 360 TTGGGGGTGA CCTGCTTCCT GGGTGAGGGC GTCTGCGAAG GCGGTTGGAG GTGGCCCGCC 420 CGCCGGTCCC ATCGGCCAGG AGAAGGGAGA CCCAAAGCCT GGGTGAGCGT CCCCTTTGGC 480 CTGGAGCCAG GGGTCAGGGG CTGGTTGGTG CCTGCCCAAC CCGTCCTGCT GGGGCTGGAC 540 TCCGCAGGAC CTGGGGAAAG CGGCCTGGGC GTGGAATCTG GAGACGGGTC CACCCTGCCT 600 GCGAGTGTTA GGGTCAGAGA CCCTCCCCTG AGACTCTCTG GGGCCCCCGC AAGGGCCCGT 660 GCGGCCTGGA GCGATCATCT TGGCGCTCCC TTCTGGAAAA GGGGCTTTTG TCCTCCAAGA 720 GCACATGGAG GCTCTGAGTG GGTCAGCCCT CCGGATCGGG AAGGGATTAC CGTTCTTCAC 780 GGGATTTAGC CCTGGCGTCT TGCCTAGGGC GTGCACCTGC CCCCGGGTGT TCTCCCAGAC 840 TCTTAAGACC TCGCAGGCTC CCTCGAGGGG CCCTGCGTGG AAGGGAAGGC GGAATCTCCC 900 TCTGATTCTG CCTGGATTCA GCACCCAGAA TGAGGTGGTC TCTGAACGCC CCTCCTCCTT 960 TACAGGCGAG GAAACAGCCC TGTGGGAAGT CGAGGTTCCA AGGTCACAGT GAGGGGGCCC 1020 TGGCCACCCG ATTCAGCGCA GGAAATAGTG AGAAAGTCGT TTTTAGCCGA CTCTGACCCG 1080 CATTCGGTTT CCAGTGCTGT CTTAGGAGGG CCGTGTGTTG AGGGTGGGCA AACGTGGTTT 1140
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