Tag | Content |
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EnhancerAtlas ID | HS047-14318 | Organism | Homo sapiens | Tissue/cell | Fetal_placenta | Coordinate | chr17:32530940-32532250 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
DUX4 | MA0468.1 | chr17:32531017-32531028 | TGATTGGATTA | - | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AAGATCTTTG TTATGCATGT GGAGAACAAG AGCTGGAGAT GGTGACCTCC TATTGAGTCT 60 AATAAGACTG GTAACACTGA TTGGATTATG TCCATATTAC AGATGAGGAC CTTGAGGTTT 120 GGGGAAATTA ACGGCCTTTC CAAAGTCACC TGGTTAATGC ATGGCAGAGC CAGAGCCTGT 180 TGACCCTATT GCATGATTTG AAATCATCAT GTTTGGGAGG CATGCACTGT GTAAGAAGAC 240 AAGGAACTGG AGCCAGGATG CCAACTTCCT GAGTGACCTT GGGCACATTA TTTGAGGGCC 300 TCCATTTCTC TATTTGTAAA GAGTAAAGCT GGATGAGATG TCTCAAAGTC TTTTCTGTTC 360 CCACTGAAGG TCTGTTGCTG CAACCCCATT GGAGCTGATG ACAGACTCCA TCAGCTGGAA 420 GTCTGCTCAA CCTGCTCCAC CTGCTCTACC ACCTCCAGTA CCTGGAAGTC CAAAATTAGG 480 AGAACAGAGC CCACGGCCTC ATGCCACCAC ACCTGCTTTC ACCAGCTCCT GGAGAAGTTG 540 GACAGCTAGA GAAGGGAAAG CATGCTGGGC TGGAGCCCAG TGGGGTCACA CTGTGGGCTC 600 CCTGCTACTG TCCTCTGCTC CAACCTGGCC AGCCACCAGC TCGGCCCTGG GGTGGGGAGA 660 GGTGGCATCA ACAGTCAGGA GCTGCAGCCT GGGGGCTGCC CTGCCCTGCA AGGCTTCTTG 720 CTGTATGTCA TTCTTGCTGT ATGTCCTTGC ATGCGGCCTG GCCCTGCCTT AAGCAGGGGC 780 CTGCTCCTGA CAAGCAGCTC AGCTAGGGAG GAGAGGCCAT TGCAGCAGAT GGGCGGATGA 840 AGACCAGGTG GGAGCATGAG GCCAGATCAC GAGAGTCCTG AGCCCCCCAT GGAAGACCGT 900 TCCAGGCCAT CCCTGGCCCT GAGTGTCATC TCCCACTATC CCTGTCACTA AGGTCCCCCA 960 TAAGTTTGAC TTTGCAAGCT CCCTCCCCGA GATTTAGGCA TCCTTGGGAC TTAGCTCCTC 1020 TCTCTAGCAC CCGCGTGCAC GGAGTCCTCC CCATCGCCGG AGCATGAGTC CATGCTTGAG 1080 ACTAAGCCTT CTCCCCATGC CTGGCACTGA GTGCCATCCA CGTTATGATG TGCAACTGAG 1140 CCCTGACATT GAGTGGCCTT TACCTACCTG ACACCTAGCA CCCCTGATGT CCCATAGTTA 1200 GTGCTTCCCT GATAGAAGAA TGCCTCTTAT CCTCCTCAGC AGGTGGCCTC CCTCCCACTT 1260 TGGCAGTCTC TTGCTGTGAC CCTAGCCCCA CTTGGCGTGT CATCTCACCA 1310
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