Tag | Content |
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EnhancerAtlas ID | HS061-11814 |
Organism | Homo sapiens |
Tissue/cell | GM12892 |
Coordinate | chr19:2123870-2124820 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr19:2124723-2124738 | GAGGTCAGGAGTTCA | + | 6.22 | REST | MA0138.2 | chr19:2123895-2123916 | GTCAGCACCACGGTCAGCACC | + | 8.73 | REST | MA0138.2 | chr19:2123907-2123928 | GTCAGCACCATGGCCAGCGCC | + | 9.97 | ZNF263 | MA0528.1 | chr19:2123970-2123991 | GGAGGAGGGATGGGAGGGAGG | + | 8.57 |
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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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| Number: 1 | ID | Chromosome | Start | End |
GH19I002123 | chr19 | 2123781 | 2123930 |
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Enhancer Sequence | GATGAGCACT GCAACAGACA GCTTGGTCAG CACCACGGTC AGCACCATGG CCAGCGCCGA 60 CACCAACTCA GGGCCACGGG GCACCAGCAC CCCCTCGCCG GGAGGAGGGA TGGGAGGGAG 120 GACAGAAATG CCACTGAGTT TGGGACCACG CAGCCCAACT GTGTTTGCAA AAACCTAGCT 180 CCATCACAGG CCTGAGGATA GGAACCTGCA GGGGCCCCCA CCCTCACTGA CAGGATGGCT 240 CGGGGCCTCA GCTGTTCCTG CAAACACTGG TTCACTCGCA ACCCCTGCTT CCCTCTGGAG 300 TCTGGAATCC CGGCAGGGGC CAGGCCCCGA GGCCACAGGA CCAGACCCTG TAGGAACCCA 360 GGCGCTGGGT CTCTGGGAGC CTCCATGGTG ACACTTCACA AATTATCATC ACAGCTCACT 420 GCTGGGGGAT GAAGCACATC CGGCAGGACT CCACTGAAAG AAGGCTCTAG AAGCTGGGCC 480 TGGCCTCCCC AACATCCCCG GAGCCATTCC CCTTTGCTGA CTCTGCTGCG TCCTTTGGGC 540 AGGGACAGGC AGGCAGCGAG AAGCCGACCC TCAGAGCCCC AGCTCTAACA GCTTTAAAAG 600 AAAGACATGA AGCCAGGGGA CCGCCAGGCA CATGCAGGGA CAGAGACTCA TTTTCCACCA 660 AGCCAGTGGC ATGGAATGAA GGTGTACAGG AGACCGTGTG TGCGTGTGCG TGTGCATGTG 720 TTTTCTTTTT AAGACATGGG TTCTTGGAAG CTAAGCTATG AGGACGCAAA AGCATAACAA 780 TGATCTAGGC CAGGCGCGGT GGCTCATGCC TGTAATCCCA GCGCTTTGGG AGGCTGAGGC 840 GGGCAGATGA CCTGAGGTCA GGAGTTCAAG ACCAGCCTGA CCAACATGGA GAAACTCTGT 900 CTCTACTAAA AATACAAAAA TAAGCGGGAG TGGTGGAGCA TGTCTGTAAC 950
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