Tag | Content |
---|
EnhancerAtlas ID | HS139-29152 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr2:71098080-71099760 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr2:71098795-71098814 | CGACCAGCAGAGGGCAGCA | + | 7.76 | Myog | MA0500.1 | chr2:71098844-71098855 | GACAGCTGCAG | + | 6.62 | Tcf12 | MA0521.1 | chr2:71098844-71098855 | GACAGCTGCAG | + | 6.14 | ZNF263 | MA0528.1 | chr2:71099412-71099433 | AAAGGAGGGTGGGGCAGGGGG | + | 6.08 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH02I070871 | chr2 | 71098549 | 71099186 |
|
Enhancer Sequence | AGGATTGGAA GCTGAGGAAA AGGGGGCGTG CATCCTGGAA CAGAGCAGAT GCAGATACAC 60 AGAGTTGAGC TGTTCTCCGA CTCTTCTGTT CCCAGGGCCT CCTCCTAGAG AAAGCCCAAC 120 TCCTGTGGAT TATACCAAGC CTTGCTCAAG TGCAAGCTCT CCCTGGCTCC TGATCCTCCT 180 GGTGCCAGGC TCGCCCTTTA CAGCCACAGT TATTTTCGAA TGCATCACCC GTATAATCTT 240 CCTATGTCTA TCTCCCCTAC AGACACTCAA AATGGCCTCT AGTCACTAAG AGGAAGAGGA 300 CAGTGACTGA CGTCTGGCCA CAGGGGTACC CTGGGGTGGG AGCTGCCGTT GTTCACTACA 360 GCAAGGTGGA TGTTTTCATT ATCATTGTAC CCCCAGTACT CAGGGAGTAT TCCGGGAGCA 420 TAAAGGACTC CTCTTGGGTT TCCCATCCTA ATGGGGCTGT CCGTCCTGCC CCTTCCCTTA 480 TGGACCAGGA TTAGGGAGCG TGGACTGCTG CACTGGGCAC GAACAGGTGT AACCAGAGAA 540 ATTAGACACG CGGCCAGCTT CCCGGGCCTG GCCTCGTTGG AGACATCCCC CACTCTCCCT 600 CCTTTTCCCA CCCCCATCCA CCCATTTCTG GACCCTAGGG AGCCATAGCC CACCACCCGG 660 GGTGCCTGCG CAAGGAAGTC GGCGAAGAGC GAAACCCCTC GGTGCTGTAA GTTTGCGACC 720 AGCAGAGGGC AGCACAAGGC CGCTTCCCTG GAGGTGGCCG GCAGGACAGC TGCAGCACTA 780 CTGGAGGCGG GCGGGCACCG ACTGGCGGCG GCCAGGGTAG GAGAGCCCTG TCAGTGTGAA 840 ATTAGCCTGA AGACTGGGGC GTGGTATTAG TGCGTACGCC AGGGGCACGT CCCGGTCCCT 900 GACACCCAGG ACACTGTCGT TACCGCCGCC TTCCTCCATC AGTGTGGTAC CAAGGGCCGT 960 GTGGTGCAGT GATGGGGGCA CAGGCTCTGC CATGAGGCTG AAAGGATGTT TCCACTCCAC 1020 CGTTTACTGT GTGGCGTTGG GAAAGTTACC TGACCTGTCT GAGCCTCAGC TTCCCCATCT 1080 ATTACATGGG GTAATACGGC CCACCTCACT GGGTCGTTAG GGAGCTCATA GGCACACCGG 1140 TAAGTGCTTA ATATTCACCT TCATCAGCAC TTTTCTTATT GCGTCATAAT TGCCCAACTG 1200 TGTATCTCTC CTTGTACAGG TTTCCTTAGC ACTTGTGGGA GATTATGTTT GGGATCTATA 1260 TCCAGGAGTG GAATTTCTGG GTCACATGGC ATGAAAAAGT TCCCAGATGC CTGAGCTGCC 1320 TGGTCCTCAG GAAAAGGAGG GTGGGGCAGG GGGGTGTCTC CAATCTCAAA ATACCTGTCA 1380 GGCATTTTGG GATTACAGTG CCCAGCCCCG TCCCTCATCA AAGTAACTGC TCCGTGAGCT 1440 GTTGTGAAGC CAAGCTGAGT GGGAATGAGG TTGCCACAGC TCTACACTGG GCGCTACACA 1500 GCCCCTGGCT GACCTCAGAC CCTGTCCAGA TCTCCTCAAA CTCCAGCCCC TTGGAGCCCC 1560 CTGGTGTTGG GAACAAGACC CCCCAAATCT GGCCATAAAC TGGCCCCAAA ACTGGCCATA 1620 AACAAAATCT CTGCAGCACT GTGACATGTT CATCATGGCC ATAATGCCCA CACTGGAAGG 1680
|