Tag | Content |
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EnhancerAtlas ID | HS139-11150 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr11:125826040-125826710 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
E2F6 | MA0471.1 | chr11:125826411-125826422 | GCTTCCCGCCC | - | 6.02 |
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| 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 |
GH11I125956 | chr11 | 125826002 | 125827202 |
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Enhancer Sequence | AAGAGGACCC ACAATGGGGA GACAGGGATC TCTGGGTGTC TGAGGGCAAG TGAAAGCCAT 60 GGTACTGGGA AGGATCTGTG GTGCTATAGA AGTATGAGCA AGCTAGCTGC TTCCAGAAAA 120 AAAGTCTGTG GATGGAGCAA TTCCTAAATA AATCAGAGCT GATGTTCACG CCAATAGAGG 180 GCTACTTCCA TTGCGACTCC CACAGAGACA GGCTGATGGC TGGGTCCCAG GTTTGGCTAG 240 TGGGAAGAAG CAAGGTGTGT AGGTGTGTGT TCCTTTGCTC AACCATAGCT TACGAACATC 300 ACTGACGCTG CAGTGGTCCG ACTCCAGGAG TCGCAGCCCA CAAGATACGG AGCAGAGGTA 360 CTGCAGATGT AGCTTCCCGC CCCCAGGCTG GGGGAGCTGG CCCACAGAGC ACCGGGGCTG 420 TTCCAGAGTC ACAATGTCAG CTGCCAGCAT GACTCACTAG CTCCAAGTGT GTGTGTCTGT 480 TTGTGTGTGT GTCTGTAATC TGGGTGAAAA CACAAATGAA TGCTTGTTCA ACTGACTAGA 540 AGACTCGGGA CTCCGAGCCG CCTCTGCAGG AGACACAGAT GAGAAGAAAC GGCAAGAAAG 600 CCAACGGGGG ACCCGCCAGC ACAAGGGACG TGGCGCCTGA AAGGAGACAG AAAATTGAGA 660 AGCTTAAGAA 670
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