| Tag | Content |
|---|
EnhancerAtlas ID | HS139-11708 | Organism | Homo sapiens | Tissue/cell | Myotube | Coordinate | chr12:9620740-9621870 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr12:9620899-9620918 | TGCCCAGAAGAGGGCACTG | + | 6.44 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr12 | 9621303 | 9621405 | | chr12 | 9620782 | 9620989 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH12I009468 | chr12 | 9621397 | 9621997 |
| Enhancer Sequence | TTTAGTTTGG CCTTTCCTGA CTGGGAAAAC ATCTAAACAT GGTTTCTTAA ACTGTTTAGG 60
CTGTAACCAA CAGACATAAA TATATTTTCT GGTGACACTT AGTGCACAAA TACATATATT 120
GACAAACAAG TGTTTTGTGA CACTACTATA AAATAAAGCT GCCCAGAAGA GGGCACTGGT 180
GGCAAATCTA GGCCTGAGAT TATTTTGACC TTGCTGGAAT TTTTTGAATA TTTTTGCTGC 240
ATATCTAGAT GCATTAGAAG GTTGTGGCAT CCATTTGGCT TTTAAATGCC AGCTATGAGA 300
GAGGAGGTGG CCGCAGCACT GGCTAAAGGG CAGAAGGAAA AAGGGAAAAT TCTCCTCCAA 360
GGGAGCAGAC CAATGTTGCT TAGACCCTAG CTCTGATCAC CCTTCTCTCA AAACTCTGCA 420
TCCAAACCTC ATCCTCAGGT TGATCTCTTC TACCCTTGAC TGCTCTGTTC CCAGATGTAC 480
TGGGTTGAAA AAGTTCATGT CCACTCAGAA CCCGGAATGC GACCTTGTTT GAAAATAGGG 540
TCTTTGCAGA TGTTACCAAG GTAAGGGGAG CTCAGTGGAT AAAAGTGGGC CCTACTTAGT 600
CCAGTGATTG CTGGTTTTAT TAAGAAGAGA ACACACACAC AGACACACAC GCACCAAACA 660
CACACACACA CATATACACA AGAATGTGCC CTGTGAAAAT GCAGGCAGAG CTTAGAGTGG 720
CCTGGATCTG TATGTTGCTT CAGTTCTGGG AGCTCCCATG AGCCTGCAGA GAGATTGCAG 780
GGTCTTCCTG AACAGTTCCT GAGGAGGAAA GAGAGACTCA GAGGATTGCC CCGATGTCGC 840
CCTTCTCTCC TCCTAAACTC TGCTGGGCTC TCCCACTCCC CCAGGAAGAC TTCCCTGCTA 900
ACTTCTGCCC TGCAAGTTGA CCCTGACATT TTCAAGTGCC ACCTGCCCCT GTGAACTTGA 960
ATGGATTGCG CTGTTCTTTG CACAAGAGCA GAAACGTCTG CCTGGAGTGC GGCTTGTCCT 1020
AGTGGCTGGG ACTTCCCTGA CACACAGCTC CCCCTGTCTG CCATGGAGTG GTCTCACTGA 1080
CATCTGGGCA AACAACTGGA AGAAGCTACA GCCCCAATTC TAAAGGTTCA 1130
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