Tag | Content |
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EnhancerAtlas ID | HS139-56456 | Organism | Homo sapiens | Tissue/cell | Myotube | Coordinate | chr9:101191520-101193340 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Zfx | MA0146.2 | chr9:101192328-101192342 | GAGGCCGAGGCGGG | - | 6.01 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr9 | 101191829 | 101192324 | chr9 | 101192837 | 101193200 |
| Enhancer Sequence | AAGCGATCCT CCTGCATTAG CCTCTTGAGT AGCTGGGATC ACAGGCATGC ACCACCATGC 60 CCAGCCAATT GTTGTATTTT TAGTAGAGGA CCGGGTTTCA CCATGCTGGC CAGGCTGGTC 120 TTGGACTCCT GACCTCAAGT GATCCGCCCA CCTCAGCCTC CCAAAGTGCT GGGATTACAG 180 GCATGAGCCA CCACGCCTGG CCGGATTTTG GTATATATTT TTGTCATCAC ATTTTATGGT 240 TTTAGATTTC TGACTTCTAT GTCAGTGACC TCGCTACGTA CATGCCTTTT ATTGAGAACT 300 GCTTCAAACT CTCCTTAGAA GTAGGCGATA CACTATGATT AATTTTAGTC AAACAAGCAA 360 ACAAGGCATG GTGGTTAGGA AGATTTTCCA AGGTCACACA TCTTGCAGGC AGTGGATTAC 420 AGGAAGACAG GACCAAAGCT TGTTGAGGAC AAGCCATTCA CTCAGTGTCT TCCCAGGGAC 480 TTCAGAACAA AGCAGGGGAG CTTTTCAGTC TGGAAGGGGA GGCGAGAAAA CAGATGTCTT 540 CTCTTGACTT CTGAGTTGGC CACAGTCCTT TTAAGTAGCT TACTGGGATG ATGCAATCTA 600 GATTTCTCTG ACATTGTCTC CAACTTCCCT CCCCCTTGCT GATACCATTC CAGCCACACT 660 GGCTTCCTTG TCATGCCCAC ACACTCCAAC TTCTTTGCCT GCCTGGTAAT TTTTCACTGG 720 ATGTCAGACC CTTCATTGGG TGTTAGCTTT TAAAAATACT CCTTGAGGCT GGGCGTGGTG 780 GCTCATGCCT GTAATCCCAG CCCTTTGGGA GGCCGAGGCG GGTGGATCAC AAGGTCAGGA 840 GATCAACACC ATCCTGGCCA ACATGGTGAA ACCCTGTCTC TACTAAAATA AAAATAAAAA 900 AATTAGCCGG GCTTGGTGGT GCACATCTGT AGTCCCAGCT ACTTAGGAGG CTGAGGCAGG 960 GGAATCGCTT GAACCCGGGA GGTGGAGATT GCAGTGAGCC AAGATCATGC CACTGTACTC 1020 CAGCCTGGCG ACAGAGCGAG ACTCCGTCTC AAAAAAAAAA AAAAAAAAAA AAGTTCCTTG 1080 AAATATTCTT AAGTTCTGTC TGGGACATAA TTAAGTTACT TGGAAGGAGT TTGACCCTTT 1140 CGAGTCTTGC TTTTAAGCTT TTTTAGGTGG GACCAGAGCT GCCTTTAGTC TAGGGTTCAT 1200 TTCACCCCAC TCCTGAGATG ACCCCCTTCT GAGTATTCTC CTTGTGATTT ATTAAACTTT 1260 TTCCCACCCA ACGTGGTGGG AACATGAACT ATTCCCAGGC CTGCCTGAGC TCTGAGGATC 1320 CTTCTGCCTG TCTTTTCCTT TCTGCTGGTT CTTTCCCTGG TCTCAAGTGC TTTCCTCTGT 1380 ACATGTGCCA GTAAGTACTC AGCTGAGGGT GTGAGCAGAC CTGCATAGTT CTCCCTCTCC 1440 ATGCAGCTCT CTCTTCTCCA GTGCTCTGCC TGCAAACTTC TGCCTCCTTT GTCTCTGAAT 1500 TCTCATCTCT GTCTCTGCAA CTCAGCAAGA CTGCCAGGCT CTGTTTGGGT TCCCCCTTCC 1560 TGTGCTGGAA ACCCTCCAGA TGGTCATCTG GGCGATTGTA AGATTCACTT CCTTTGTGCT 1620 CCTCCTCTCA GGGGTCACTG TCCTCTGCTG CTTGTAGCCC ATGTCTGAAA ACTGTCATTT 1680 CACATAGTAT TTGGACTGTT TTTTTTTTTT CTTTAACTTG TTTACAGCAG GAGGGTAAAT 1740 CTGGTCCCTA TTACTCCTCC ATCTTGGTTG GAAGTGGGAA GTGGAAGCCC CCAACTCCAG 1800 AACTCCAGAT ACTCTCACCT 1820
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