Tag | Content |
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EnhancerAtlas ID | HS098-22064 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr16:66642370-66643330 |
Target genes | Number: 15 | Name | Ensembl ID |
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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) |
CTCF | MA0139.1 | chr16:66642612-66642631 | TGGCCACCAGGTGGCGCCG | + | 9.55 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH16I066607 | chr16 | 66641721 | 66643461 |
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Enhancer Sequence | AGGACAGGGG CCCCAGGAGG GAGGGGTGCC CTGCACAAAG TGGCCAGATG AGGAGTCCAG 60 AGTCGTGCAC TTGGGCCCTT ATCCTTTCTC TAGTGTGCTG GAGTTTGCAG TTGGTTAGAA 120 CTGGATGGAG AGACCCAGCT TCAGATCATC CCAGCTCCAC TACTCAGCAG CCCTGTGACC 180 TCAAGTGGGC TGTGGTGCCT CTAGAGCAGG TCTGTGAGGC AGGGAACCCG GAGAGGGGTC 240 TCTGGCCACC AGGTGGCGCC GGTGCTCCCC ACCGGGCCTA CAGGAATGAG CTGCCGCCAC 300 AGGAATTCAA GCCATTTCCA CGTGGGCAGG ACAGGTTAAC TGAGGACTTG CAGGGCTTAC 360 CCAGACTTCA GCCATCGGCA ACCCTGACCT CGTTTTATCA CCTGTGAGGG CCCAGACCCC 420 AGTGGACCTC GCTGAATGAA ATGTGTCCTA GAGAAAGGGC AGCAAAGGCT CAACTTGAAC 480 CCTTGTCTCT TGACTTCATA TCCAGCATCT GCTGCCTCAG GAGGGCTGCA CCCTCTGTGT 540 CCCCATCTTA GGGACGGATA AGCAGAAACT GTGGTCCATG AATGGATCGG CCACAAGAGT 600 GTGACAAAGC CGAGGCCCAG AGCCAGATCT CCCCAATGGA GAGCGGGAAG GGAGCAGGTG 660 GGGGTGTTTC CAACTTCTGC TTCCACCGCA TCGCAGGGCA GGCTGCACCC TGATCCACAC 720 AGTTTTTTGC CCAGAGCTTA GGACAGCAGC CCCGCTGGAC CCGGGATAGG GCAGTGTCAG 780 CTGCTGGCAA GGCAGCAGAG GCACCTCGGG GGTGGGACAA GGGCCTAGGC ATGTGGGTGG 840 GGCCAGGATG GGATAGGAGC CCTCAGGTGC TAGGCCTGGG GCTGGGAACA CGACCAGGCT 900 GCCAGGCCTC CTCCCCATGC TGTGCTCAGC TCCAGGGGCT CAGGGCAGCA TGCCCCTCTC 960
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