Tag | Content |
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EnhancerAtlas ID | HS139-08620 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr11:8937500-8938830 |
Target genes | Number: 10 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr11:8937721-8937736 | TGAACTCCTGACCTC | - | 6.22 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I008916 | chr11 | 8937667 | 8940389 |
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Enhancer Sequence | TGGGACTACA GGCGTTGCCA CCACGCCTGG CTAATTTTTT GTATTTTTAG TGGAGACGGG 60 GTTTCGCTGT GTTAGCCAGG ATGGTCTCGA TCTCCCGACC TCGTGATCCG CCTGCCTCGG 120 CCTCCCAAAG TGCTGGGATT ACAGGTGTAA CCCACCGCGC CTGACCCATT TTTGTATTTT 180 TTAATAGAGA CAGAGTTTCA CCGTGTTGGC CAGGCAGGTC TTGAACTCCT GACCTCAGGT 240 GATCTGCCTG CCTCAGCCTC CCAAAGTGCT GAGATTACAG GCGTGAGCCA CCATGCCTGG 300 CCCCTGTCTT TCATAATTTT TAAAAAGAAA GTACAAGGGA AGTGTGGGGA CGGGGGTCTC 360 TTTTAACAAA ATACTTTTTG TAAAGGTAAT AACAGTTACG GGCCTCTCAC TACAAACTTA 420 CCTTTTACCA CATGTCATTC TGGGGAAGCC AAAGATTCTG CTTATTGAAC TGATTCAAAG 480 GAGGAGGTGG TGGTGGTGGT TTCTGAGGAG ACTAGGTTTT TGCTTTTGTT TTAACCTACC 540 CTACTTGTAC TCAAAGATAG CAAACTGAAG TCCAGAGTCT ATTCCAGAGT CTAAGTTGGA 600 TTCCTGACTT CTTTGGTCTG TCAGCCATTT TGGGGTGTTA GAGGGAGGAA GTTTAGGAAA 660 AGGATGGGAG AGTGGGCACA GGGACATGAG CAAGGGCTGA GTGCACACTC GAAGCACCTC 720 CCACATGCCT CCCCTGGCCT GGGAGGTGAG TAGTGGTGCC AGAGCTTGAG TCCTGAGCCC 780 CCTTTTCTGG CCTAGCCTGA ACTCTTACCT AAACGCACCT GACCCTAAAG GGTGCACTTA 840 GGTACATGTG GGGAAGAGTC GTTCCCATCT CTCCCTTTAA AATGTAAGTT CCCTCTAAGG 900 GAAATTGGCT TTATCAGTCA GCCTGTTCCC TTCTAGGACC ACCCCCACTC CTAGAAGAAG 960 CACAGAAGAG AATGTATTGA GAGCCTAAGT GCCACTTTTG CACTTTAAAT TTTCCCTGCA 1020 ATCCAAGAGT GCCATGTTAC AGACTGGAAA ACCAAGGTTC AAGAGAAGTT AATCTGTCTT 1080 AGTAAATAGC AGAGATAGGA CTTAAACTCA GGCGTGGCTG ATTCCAAAGC CCATGTAAGG 1140 ATGAAAATTA TAGTAAATAC CTGACTAAAA ATACCTCACA GAATTCACTT AAAAATGCCT 1200 TAATGACTTA GATGACAACT TAGAAAAAGC TGACAGAACA ATTACTAACT CCTAATAAGG 1260 TAGAAGAGAA CTTCTCTTTA CAATCCAAAA GTGAAAGCTT GGGCACAAAT CAGTGTTCTA 1320 CTTGTCTCTT 1330
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