Tag | Content |
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EnhancerAtlas ID | HS098-58280 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr9:113995320-113996700 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Klf1 | MA0493.1 | chr9:113995972-113995983 | GGCCACACCCT | + | 6.32 | Nr2f6(var.2) | MA0728.1 | chr9:113995828-113995843 | TGACCCTTTGACCTC | - | 7.29 | SCRT1 | MA0743.1 | chr9:113995744-113995759 | GTCCACCTGTTGAAT | - | 6.39 | SCRT2 | MA0744.1 | chr9:113995746-113995759 | CCACCTGTTGAAT | - | 6.62 |
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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 |
GH09I111232 | chr9 | 113995241 | 113996874 |
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Enhancer Sequence | AATTTTGCTT CTTAATCTCA CACATCAAAA AATCTTTCTC TAATTCAATT GAGTTGGCCA 60 GTTCCAAGTC CTAAAAAATA GTGCTAAATA TCTGGAATTC AGGACTGGCT GCTGTGGCTC 120 ACACCTGTAA TCGCAGCACT CTAGGAGGCC GAGACAGAAC TTGAGGCCAG GAGTTGGAAC 180 TGCAGTGAGC TATGATCACA CCACTGCACT CACACCACTG TTTTGTTGAT TAGGTTAATA 240 TTCGTCCCTT AAACCATCAT TTAGCAAATG AACACTGAAG TAGAATATCC ACCAAAGGCA 300 AAACATAAAA ATTAAAAAAA AATTAAAAAA AGAGATCCCT TAAACGAGGG AGGAAGTTAT 360 GAAGTGATGA GAAAGAGCTG AGGGAATTTG TTGACTGGCC CAGCCCTCAG CTAGATTCAA 420 TCCAGTCCAC CTGTTGAATG CCAAGAAAAA TAAGTGCATT TTGCAGAGGC TGAGATCTCC 480 AGCTCTCTCC TCTGACCTCC CTCCTTTCTG ACCCTTTGAC CTCCCCTGCA GGAGCCGCTC 540 TGAGCAACTG TGCCCAGCAC CTGGGAGGCG AAAGAACCCT GCAGAAGCCA ACAAATCAAC 600 ATTCCACCAG GAATTTTGTG CTGGATAATT CAACCAATTC AGCTGTTATC CTGGCCACAC 660 CCTCGGTCTG GGCTTCCATC CAAACTTCGT CCTTCTTCAC TGTTGAAAAC CAGAAGCCAC 720 AGCCCCCAGC CCTGTCTTCT AGCTCCCCAC CCAGGCCCCC CTCTCTCTCT CTGAGCCTCT 780 CCACTGTGCC TGGTAAAACC CCAATTCTAT AAGGAACAAA CTTCCTTTGG TCTACAAATA 840 TTTCCTTGAG AATTCCCCCA ACATTAATAA AAAAATCTTC CGGCCAGGCG CTGTGGCTCA 900 CACCTGTAAT TCCAGCGCTT TGAAAGGCCA AGTGGGGAGG ATCATTTGAG CCCCAACAGT 960 TCAAGACCAG CCTCGGCAAC ATAGTGAGAC CCTGTCTCTA CAAAAAATAC AAAAATTAGC 1020 CAAGTATGGT GGTGCATGCC TGTGATCCCA GTTCCTTGGA AGGCTGAGTG GGGAGAGTCA 1080 CTTGAGCCTG TGAGGTCAAG CCTGCAGTAA GAGGAGATCG CACCACAGCA CTTCAGCCTG 1140 GGCAACAGAG TGAGACCCTA TCAGGGAAAA TAGAAATGAA CTACTTAGCT TTCTTCCAAA 1200 ACCTGCAATT CATGAGGAAT AATCATCCTC TTAATCAGCA GGGCACCAAC ATTTGGAGTG 1260 AACACGACCT TCTCCCATTT GCCTTCCACA TACCATCTGT TGCCAGACCT TGACAATTCT 1320 AACTCTAGGG ACTTTGTGCA AGGGAATGGG GCCTAAATGG GCCCATGCTC AATTATTAAT 1380
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