Tag | Content |
---|
EnhancerAtlas ID | HS139-53454 | Organism | Homo sapiens | Tissue/cell | Myotube | Coordinate | chr8:59445370-59447700 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Tcf12 | MA0521.1 | chr8:59446234-59446245 | CAGCAGCTGTT | - | 6.32 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CAGTCTCTCT CTCTCTGTGT GTGTGTGTGT GTGTGTGTGT GTGTGTGTGT GTGTGCTGAG 60 CTGCCTGGGT GGGGAGTGGA GTTGGGGGTG GACACAAGCA CCCCTGTGGC CACCAATACT 120 GGGACTGCAC TGGGTCAGAC CTGAAGCCAG CACAGCACTG GGTCTTGCCC ATGGCCTGCC 180 ATAACCACTA CCTGGGTACC ACCTATGTTC ACTCAAGGCC CTAGAGCTCT ACAATCAGCA 240 AGTGGTAAAG CCAGCCAGGC TTGTGTCCTT CCCTTCAGGG CAGTGAGTTC TCCCAGGCCT 300 CTGGCAGGTC CAGAGATGCT ATCTAAGAGC CAGGGACTGG AATCAAAAAT CTAGGAAGTC 360 TATCTGGTGT TCTATTCTAC TATGGCCAAG TTTCTCCTCA AACCATGGGG CACTTTCATG 420 GGAAAGTACT CCCATGGGCC TGTGGTGGTC GTGGCCATAG AGTGAGGCTT CTCTGCCTGT 480 GGAAAGGGGA GAGAAGAGTG GCAAGGACTC TTCCCACTCA AGGACTCAAA TTAAAGGGGA 540 GAGAAGAGTG GGAAGACTCT CCCCTTTCCA CAGGTAGAGA AGCCCCACTC TATGACTACC 600 ACCACCATAG TCCCATGGGG AATACTGCCA GTCCACTGTA GATGTTCACT TAAGGCCCCA 660 AAACTCCTCA GTCAGCTGTG GTACATACTG CCAGGCTTGC AACTCACTTT TCAGAGCAGT 720 GGGCTCCCCT CTGGCCCAGG GCAGATCCAG AAATCTGGCA GGTGGTATTG CTTCAGCACT 780 ACTACTCACT GTGGGGCTGG TAACTGTACC AATGTCCATT CCACATTCCC TCCACCCCAA 840 TCACATGCTT CATTTGGAAT TCCCCAGCAG CTGTTTCATG TGGGGTCCTG CCTGATAAGA 900 GAACCATTCC CAAGATGTGT TCTGGGATGG GAGCTATGTA TACTAAAAAG AGTTTGGGCG 960 GCTGTTTCCC AACTTTTAAT GCTAGTTCAA CCTGCCTGAC TTTCACAGCT CCCACTCCAT 1020 AGCTATCTAT TGCTGTTATA GGCACTTGGA ACCAATGAGT GTTGCCATAC ACCAGGGTGC 1080 ATTCAGCTCC AGTATCCACT AGGGCAAACA CAGTCTGTTT ATTATTAGGT GACCAATATA 1140 TAGTTAGCTC TACATGTGAC CTCCAGTCCC TGGACACCTT GGCCACCATT ACTCTTATTG 1200 GGATTCTGAG GCCTTGACCT TCATACCAGC TAAGTTAAAG GGGTTGGTGT CTGCCATCCC 1260 TCTGTGGGAG GGACAGTGGG CTGAATCTGA GGTTCCTGAG TGAACTGTTG TTGTGGCTTG 1320 AGCTTTCATC CCAGTCTAAC CAGAACAGCA TTAGGTTGCT CATCTATTTG CATGGTAGGT 1380 GTCCCTGCCA CTCATGCCAC ATTTGTCCAC AGACCACCTT AATGGGCCCC TTCACTGTCT 1440 CCTTCCCTTT GGCTCCCTTG TCTTTCATCT TGGCTATCCA CACAGCTGCC CGTGCAGTTT 1500 CTCTGGTTCC CCTAAGGCAG AGGCTGTTTG GGCTGACTGA GACTCTGCCT GTCCTACCAG 1560 GTCTCTCAGG ATAGACACTG GCATGCCCTA CCATTGGTAG GTTGCCAACT CTAAGATGGC 1620 ATCTTTCATG CCGGCAGTGA GAAGCTCATT GTAGGACATG GGTAATGCTC AGCATAATAG 1680 CATGCTTCAT CCCTAATTCC CCATGGATGT CCCGCAATTC CTCCACAGTC TGCCACTGCA 1740 AAGGAGACAT GGGGACATCT CCCTCATTTG GCCAGGGTGC CCTGCAGCCT GCAACCACCA 1800 GCTGAAGGGG ATGGCTCGAT CTCCATTACC AGCACCGCAG AGGAGCTGCC TCAGGGATTG 1860 GGGGGTTTGT GGTGCATGCC ATTTTACTCA AGTTCAGGGA GTATAATATC CTCCGCCCTT 1920 GAGTTCATAG AGGAAGACAC CCAAGACCAA CTCTGTCACC TTCTGCCTGG GCCTATTTCT 1980 CAGCTCTTTC AATTCCACAG CAGTGCTGTC CTCATTGTGC TGTGCTGTCA CCCTCCAGGC 2040 AGGGACAAGT TTTGCGGGTG TGCTCCCTGC AGGCGCAGGG CAGTCAACGG CCCTTCAAAC 2100 CAGCTACCCG ACAAACCAGG GTCTCCATCT CCATTCTGTC TGGCACCTCT AATCACAGTT 2160 TGCCCTGCAG CTGATGACCC CTCGCCTGCG CTGTGGCTCC ACCTCGTTGC TGCTAGGAGT 2220 ACAGTGAGAA ACGCCAGCCA CTGGGGCTGC GACCCTCGGG CATCTGAGCC TTGCTCAGTC 2280 AGATGCACCC CCTGCCACAA CTCTTCCAGA CTCCTCAGCG TTTTCAGGGC 2330
|
| |
|
|
|