Tag | Content |
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EnhancerAtlas ID | HS183-14201 |
Organism | Homo sapiens |
Tissue/cell | T47D-MTVL |
Coordinate | chr9:136131740-136132790 |
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 | TATCTGCAAG GCAGGCGGAC GGGGGCTGGG GGAGCCGCCG GCCGTGCACC CCTGGGCTGC 60 AGGAGGCCCG TCCTGCACCC GCCCGCCAGC GGCCATTGGA AGGCTTAGAG CAGCAGATGC 120 ACCACGTTCT CCTGCCCTGT CCTGAGCGAG TCCTCGGGCT GCGATTCACT TCATCCTCTT 180 CCCAGCGATG GGGGACCACC AGCACCCCCT CTTACTAAGG AGGGCTGAGG GCAGGTGGCT 240 GGAGGCTGGT AGCAGGCCGC AGGCTGGCGT CTGCTCACTC CCCCTCAGCC TGGCCTGAGC 300 CACGCCTCCC CACGCAGCTG CCCCTCTTAT GGCCAGGCCG GCCACGTGCT CCCTCATTAT 360 AAGCTGCACG CGAGGCCTCC ACACACCCGC CTCTGCACCC TAGAGCTTCC TCCCTCCAGG 420 CTTGAACTGC ACCTATTCCT AAGAGTAAGT CATTCCTGGC CTCCGCCACT GTCGCTGGCC 480 CAGCTGCCCA CAGCTGCCGA GAAGTCAAGT ATGTGTCTGC GGTTGCCTGG CTAGCTCCCT 540 CTCTGGCCTG GCCCAGAGTC CCAGGGCCTT GTGGGTCAGC CACTTCCTTT GGTGTCTGGG 600 GCCAACTGCT TTGCCTGCCC CACCTACATC TGACAGAGAA GTGACCACGG CTCTGCCAGC 660 ATCCTCTTTC TAGGGTCCAA GGACAGCAAA CAGGTGTCCC CCTCCTGCTA TCTCTGGTCA 720 GTGAGCAGGA AACATCTGGA GCCTTGTATT GAGGGGGTGG CTCAGCATGA CGGCCGGCCA 780 CAGTTACAGA GAGGAGGGGG CAGCAGAAGC CACCATCCCT GGGTGAGACG CAGCCTCTGG 840 AGAAGGAGCT GGGTTTTACC GACCTGGCGA GCCCACGAGC CCACGAGCCC ACATGAGCTC 900 AGTAAGATGC TGCATGAATG ACCTTTCCCA TCTACCCTCT GGGAGGACAA GGCTGGCCGC 960 CACCCCACTC TGTCTTGAAC ACAAGGAGAG ACCTCAATGT CCACAGTCAC TCGCCACTGC 1020 CTGGGTCTCT ACCCTCGGCC ACCTCACTGA 1050
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