Tag | Content |
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EnhancerAtlas ID | HS139-57576 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr9:136131750-136132790 |
Target genes | |
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) |
MYC | MA0147.3 | chr9:136132079-136132091 | GGCCACGTGCTC | + | 6.92 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr9 | 136131982 | 136132032 | chr9 | 136132057 | 136132623 |
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| Number: 1 | ID | Chromosome | Start | End |
GH09I133256 | chr9 | 136132148 | 136133839 |
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Enhancer Sequence | GCAGGCGGAC GGGGGCTGGG GGAGCCGCCG GCCGTGCACC CCTGGGCTGC AGGAGGCCCG 60 TCCTGCACCC GCCCGCCAGC GGCCATTGGA AGGCTTAGAG CAGCAGATGC ACCACGTTCT 120 CCTGCCCTGT CCTGAGCGAG TCCTCGGGCT GCGATTCACT TCATCCTCTT CCCAGCGATG 180 GGGGACCACC AGCACCCCCT CTTACTAAGG AGGGCTGAGG GCAGGTGGCT GGAGGCTGGT 240 AGCAGGCCGC AGGCTGGCGT CTGCTCACTC CCCCTCAGCC TGGCCTGAGC CACGCCTCCC 300 CACGCAGCTG CCCCTCTTAT GGCCAGGCCG GCCACGTGCT CCCTCATTAT AAGCTGCACG 360 CGAGGCCTCC ACACACCCGC CTCTGCACCC TAGAGCTTCC TCCCTCCAGG CTTGAACTGC 420 ACCTATTCCT AAGAGTAAGT CATTCCTGGC CTCCGCCACT GTCGCTGGCC CAGCTGCCCA 480 CAGCTGCCGA GAAGTCAAGT ATGTGTCTGC GGTTGCCTGG CTAGCTCCCT CTCTGGCCTG 540 GCCCAGAGTC CCAGGGCCTT GTGGGTCAGC CACTTCCTTT GGTGTCTGGG GCCAACTGCT 600 TTGCCTGCCC CACCTACATC TGACAGAGAA GTGACCACGG CTCTGCCAGC ATCCTCTTTC 660 TAGGGTCCAA GGACAGCAAA CAGGTGTCCC CCTCCTGCTA TCTCTGGTCA GTGAGCAGGA 720 AACATCTGGA GCCTTGTATT GAGGGGGTGG CTCAGCATGA CGGCCGGCCA CAGTTACAGA 780 GAGGAGGGGG CAGCAGAAGC CACCATCCCT GGGTGAGACG CAGCCTCTGG AGAAGGAGCT 840 GGGTTTTACC GACCTGGCGA GCCCACGAGC CCACGAGCCC ACATGAGCTC AGTAAGATGC 900 TGCATGAATG ACCTTTCCCA TCTACCCTCT GGGAGGACAA GGCTGGCCGC CACCCCACTC 960 TGTCTTGAAC ACAAGGAGAG ACCTCAATGT CCACAGTCAC TCGCCACTGC CTGGGTCTCT 1020 ACCCTCGGCC ACCTCACTGA 1040
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