Tag | Content |
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EnhancerAtlas ID | HS062-03765 | Organism | Homo sapiens | Tissue/cell | GM18486 | Coordinate | chr12:49410740-49412300 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MSC | MA0665.1 | chr12:49410913-49410923 | AACAGCTGTT | + | 6.02 | MSC | MA0665.1 | chr12:49410913-49410923 | AACAGCTGTT | - | 6.02 | MYF6 | MA0667.1 | chr12:49410913-49410923 | AACAGCTGTT | + | 6.02 | MYF6 | MA0667.1 | chr12:49410913-49410923 | AACAGCTGTT | - | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CGCTGGCTCA CCCCCAGTTC TCTACATACC CCAATTTCAG TGCCCTTGCT CACACTGTTC 60 TCTCAATTTG CAGTGCCCTC TCCTAGGTCC AAAGTAATTT TTCTCTCAGC TATTCTGTCA 120 CAGTCCTCTG TTTTCATATT GATGACAGCA TTTATTATAG TCTACCTTTA AATAACAGCT 180 GTTGCTGGCT TGCCCTCACC ATCACTCCAG TTAGGCTGAA CATTTTCAAA GCAGGAGTTT 240 TCTTTCTTTT CTTTTTTTTT GGAGACAGGA TCTCACTGTG TCACTCAGAC TGGAGTGCAG 300 TGGCATGATC TCAGCTCACT CCAGCCTCCA CCTCTTTGGA TCAAGCGATC CTCCCACCTG 360 AGCCTCCCGA GTAGCTGGGA CTACAGGCAC ACACCACCAC CACCACGCCT GGGTAATTTT 420 TGTATTTTTG TTTCTGTCGA GACAGGCTTT CATCATGTTG CCCAGGCTGA TGCTGAACTC 480 CTGAGCTCAA GCAATCCACT TGCCTTGGCC TCCCAAAGTA CTGGCATTAC AGGCGTGAGC 540 CACCACACCT GGCTGAGTTT TCTTTTTCCT CTTTTTAACT TCTACCCCAG AGCCTAATCC 600 AGTACATAAA GTGTAAAGGC TAAATTAGAA AATCTATATA AAAATGCTTT GTAAACCATA 660 ATACATTTAC AAGTAAGTAG AATATGACAT GTCATTTTAA ATTTAATGGA ATTAGACTCC 720 TTATTTTTGT TTAAGATTAT CCTGATTAGT CAGAATTGGC TCCCTTGCCT GGGAGACCAA 780 CTGCGAATCA TTTTAGTACT TTGGTCGGTT TTCTTTTTGA AAACCTGAAA GAAACAACCT 840 CTCTGTGAGC AGAGAAACGG TGTGGCAAAG AATTACTCTG GGCATGTAAT CCAAAGCAAA 900 GTGAACCTGC AGTCCTTTCG TAACTACAGT AGCAGATGAT AAAAACCAAG ATGGAAAGAG 960 TTACTCTGCC TGAAAGAAGA CACATGGTTA AAAACTGTGG AGAGGGAAGT GTATGGGAGG 1020 GGTTACAGAG CGCTAGAAAA AGACTCCTGA GAGTGAGGGT GGGTGCAAAC ATGTAGCAGG 1080 CAACCCGCAG CATCTGTGGG AGGGTGACAG GGCCCTGCCA CAATTGGTCA ATGCCTGCTC 1140 GCCAAGAATG AGCTATGCCA AAACCCCTGC TTAGAGTCGC AGAGCGGGCC ATGACCTAAA 1200 ATTGTCCAGG GACACATCGG CCTCTAACAC TGCAAGATTT CCTCTTTCAA GCAAACCTCA 1260 ATTCTCGGTC TTATTAAGGG AATGTGACTT CACTGGACGC AGTATAAAGA TCTTCAGATG 1320 TCCTCCTGCC GGGGATTGCA GGGATCACAG AAAGACCATC GAGGTCCAGG AGCTACCTGC 1380 AAGCGGAGAT CCCTCTGGAC GCCCCGTGCC TCACCCAGCA AAGCCGGCTC ACAACCCTGC 1440 GCTCTCAAAC CTCTAAAAGG GCTTGAGGTG CCAATAGGAA AGGAGGCCCG AGATTGCCAC 1500 GGCATACGTG GGCCCCAAGG AGGGAGCCAG GAGTCACTGC CTGCTTGGGC TAAGGGTACC 1560
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