Tag | Content |
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EnhancerAtlas ID | HS139-19328 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr15:78909480-78910950 |
Target genes | |
SNPs | Number: 4 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr15:78910916-78910935 | TCACCACCAGGGGGCAGCA | + | 8.06 | EWSR1-FLI1 | MA0149.1 | chr15:78909480-78909498 | GGAAGGAAGCAGGGAGGG | + | 6.98 | ZNF263 | MA0528.1 | chr15:78909481-78909502 | GAAGGAAGCAGGGAGGGAGAA | + | 6.27 |
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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 |
GH15I078618 | chr15 | 78910841 | 78911170 |
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Enhancer Sequence | GGAAGGAAGC AGGGAGGGAG AAGGAGACGG TAAAAGAATC AGCCTGGTTT TACTTCCCGT 60 GGCACCACCC ATCTTGGTGA CTCCCCACCC CTGCTGCATG TGACCGAACC ACATCCATGC 120 CATGATCACA TAGTCCAACT TCTCCTGTGG GTGTAGTGCA GGAGAGAGCA CACGGCTGGC 180 TCTGCGGGCC ACCTCCTGGC ACTAGGGAAG CCACTGCCCC CATAACCATG AGCAAGCCCA 240 GCCCCTCATC AACCAAACAG GGCCTACTCG TGCTTTCTCT GGTCACTTCT AGTGCCAGGT 300 GGAGACTCCT GGACTTCATG CATCATGTCC AGGTCCATGT GCCTGTTTAC AGCCCCTGAA 360 TGGCTCTCCA GGGGTGTTTT CCAACATAGA CACTCTTTCA CCCCAAGGTT AAGCAAGACT 420 GGACTCTGAA AGATTCCGGG GGAAGAATCC ATGACCCCTG CAGGGCCCAG GAAGTGTCTG 480 GGTCCAGAGG CTGGGAGGTC TGAGTCCTGA GCACCAGAGG AGAGAGGGGT GAGGCTGCGG 540 CCACAGAGGG AACGTGTGCA TCAAGTACTG GGTGGGGCAC TGTGCCCATC TGGCTTTCCA 600 ACCTCCTGGG GATGAAGGCT GTGTGTGCTG AGTGCTCAGC TGGCCAGGCT GGCAGAAGGG 660 TCACCCGCAG GCCAATGGGC CATTATGTCT CCTGGCAAGT CTGGACAAAG CCTCCCTGGG 720 GAGGACATGT GGAAGGCAAT TTCTTGGCCT CGATCTGAAC AGGAAAATCT ACTCCCACGC 780 TACCAACAAC AGCAGCATCT TATTCTGACT TAAGAATGAG TATAGGGGCT GTGCACAGTG 840 GCTTCTGCCT GTAACCCCAG CACTTTGGGA GGCTGAGGTG TGTGGTTTGC TTGAGATCAG 900 GCGTTCGAGA CCAGCCTGGG CAACATGGCG AAACCCTGTC TCTATAACAA ATCCAAAAAT 960 TAGCCAGACG TGGTGGTGCA CAGCTGTGGT CCCAGCTACT TGGGAGGCTG AGGCAGGAGA 1020 ACTGCTTGAA CCCTGCTGGT GGAGATTGCA GTGAGCCGAG ATCACGCCAC AGCACTCCGG 1080 CCTGGGTGAC AGAGCGAGAT CCCGTCTGGA AAAAAAACTG AGTTTTTAGC AAGAGGGAGA 1140 GAAGGAGGTG TCTCAGGCAC CACCCCAGGG TTTGGGGGCA GGGCTTCAAT CTCAGGTTCG 1200 TACTCTTCTG TTGTGTGAAC ATGGAGAATG TCTTTCTCCA GGCTGCAACC TGTCCATCTG 1260 GGACTTGAGG GGTTGGGCCC TACAGTCCTT CCAGGGGGAC TGTAGGGCAG TGCATGTGAC 1320 CTCAAGCCTT AGAAGAGATA TATCTGCCAG TCAGTGGACC CCAATCTGGG TTCCACAGAA 1380 GTAAATGAAG CCTGGTCTTT AGGCCTTTCT TGGTTCACCT AAAGCAAATA AAACAGTCAC 1440 CACCAGGGGG CAGCAGTGCC TAGGGTCTGG 1470
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