Tag | Content |
---|
EnhancerAtlas ID | HS147-00837 | Organism | Homo sapiens | Tissue/cell | NHEK | Coordinate | chr1:27285150-27286840 | SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
DUX4 | MA0468.1 | chr1:27285420-27285431 | TGATTAAATTA | - | 6.62 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TACACAATTG GCCTGGCCCC AGACTCTTAT CCACTACCCC ATCCCATCTA TTACTTGGGA 60 GAAAAGAGGC AGTCAAAGCT GCCAGCTCCA TGGACCAGCG TGTGCCCAGA GAGAGCCCAT 120 GTTGGGAGCC CTGTCTTCCA GGCTCAAGCC TTCAGGAGAG TGGACAGATC TACAGTTAAC 180 CATGCTGAGC TCGGAAGTAC GTGGGGCTCC TGAGGATGGA CTGGCTATTG TCTTCTCCCC 240 AACCTCCAAA GCTTTAGGAC TCTCTATTAT TGATTAAATT AATACAACGA GGTGCCCAGC 300 GTTGTGCTAA ATGCTGAGAA AACAGCAGTG AATGGGCCAG AGGACTTTCA CCTTATTTGA 360 CTCTCACAAT TGCTCTGAAA ATAAGTAGTA TATCTCCATT TCACAGATCA GGAATCTGAA 420 GCTCAGAAAG GTGAAGTGAC TGGCCCAGAG ACACCTAGCA AGAGAGGGCT GGAGTAAGAT 480 TTGCACTGTG GCCCGCCAGG CTCTGAAGCC TGCGTACTTT GTGTGTGCCA CACATCTCCA 540 GCGGTGGTGG GATGAGAAGA GAAGACCTGG GATAAGGACA ATGCCTGCCT CAGTTCCCCA 600 CTTCCCTCCA GCCATTGAAC CCTCCTGAAG TCAAACTCAG GCAGTTTCTT CCAGGCTGTA 660 TCTCCCCGAC CCTGCTGCCA CCGCCCCGCC ACCACCCCGC CCAATCCTAG GAACCTGGTC 720 ACTTGGTTTA GTGAGGGGAG ACTCCCTGTC CCTATTGTGG CTTGAGGCAA GATTCTTAAC 780 CTCACTTTCC TCATCTTTAA ATAAGGAGAG ACTAGTATCT TCATGCCCCG CCAATCCCGT 840 GAGATTTAAA TGAAATATTG AGTGCAGGGG GCTTCCCGCA GTGGCCTTGC CCATGGGAGG 900 GGCTAGGTCA CTAGGCGATC TAAGGCACCG CAAGGATGTT CCCGGGGGTC AGAGGGTCCC 960 GGCCCGCCCT CCCTGGATTT CTCGTTGATG CTTTCCTCTT CCCCCTTAGT CCCGCGAACA 1020 CACACACACA CTCAAGGGTC TATGTACCGT CCCCTCCTCC GAGGGTCCCC AGGACAGGCC 1080 CGGCCGCACC AGCCTCTGCC CCCAGCCCAG TGCCAAGCCT CGGACACCCG GCCGGGGAGG 1140 ACCACCCCAG TCCTGCTCGA GAAACAGCCG TCGGCTCAGT GCACCCTCGG CCTCCTGCCC 1200 CAAAGGTGCA GCCCGAGAGT CCCATATCCG CGGGCAGCTA GTCCTGGGGA CAAGGAAGAA 1260 CCAGATCCTG GCACTGTCCC CCGGGCTACC ACAGCCCCTA CACCAACTCT GCCCTCGGGG 1320 CGAGCACTAC CCTCTCCAGC TGCAAGGGCC CTACCCCGCG GGCGGACCCA GCCTCCCTCC 1380 CGTCCCGACG CTGTTCCTCG GGGTGAGCAC CAGCGTTTGT CCCATCCCGA CGCTGCCCCC 1440 CGGTGAGTGC GGCCCCCGCA CCCAGCCAGT GCAGCCCTAA GGGCGAACGC GGCCCCTCAC 1500 CCCATTCTGC GCGCCCAGCC CGGGCGCCCG CTCAGGCCGC TCCCCAGCCC GGCCCGCGCA 1560 CCCCGGAAGT AGGAGGGTGG CCCCCGAGGA ACCGGGCCCG GGACCCTCTC CTGTCCGGGC 1620 TCAGCTTCGG GGGGCTCCCG ACACCGGCGC CGCCCTGGCT TGCGCCCCCC TGGGCCCGCG 1680 CCGGGCTTAC 1690
|
| |
|
|
|