Tag | Content |
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EnhancerAtlas ID | HS047-07184 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr11:129565520-129566430 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
E2F6 | MA0471.1 | chr11:129566095-129566106 | GGGCGGGAAGG | + | 6.62 | Nr5a2 | MA0505.1 | chr11:129566019-129566034 | GGTGGCCTTGACCTC | - | 6.78 |
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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 |
GH11I129695 | chr11 | 129565423 | 129566399 |
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Enhancer Sequence | AGCTTCGGAT GGAACCTGCT GTGTTCTGTC CTCTTCCAGC TGAGCCAGGC CCGCGGGCCC 60 CCTCCAGGAG CTCCGGGCAA GCAGCCCCTC ATGGCCCGTG GTGGAACTGC ACCCTCAGCA 120 CTGGAGAGGG CGGTCGCAGG AGCCTGCGAG GAAGGTGGGG TCTCAGTGCT TTCGCACAGG 180 GCGAGTGGAG CTGGAAATGC AGCCCCCAGT AGTTTCAGTT ATTCCATGTA TGGCTTTTCT 240 CTCTCACCTT GCACCTTTAG ACCCTAATTT CCTGTGAGCA ATGTGCTGGG AAAACTGGCA 300 GCAGCTCTCT GGCAACCCTG GGGGAAAGAA GCGAAGTGGG GTAGAAGCGG AAGCCAGGGG 360 CAGAGGCTGG GTCGGTCCAG CCAGCCCGCG AGGGCTCCCA CGCAGCAGAG GTTCCACTGA 420 GAGGAAGCCG GGGCTGGCCC GGCCGGGAGA CTCCCTCCAC GCCCCGTGTG TGGAGTGCCC 480 GGGCACCCTA TACCCTCAAG GTGGCCTTGA CCTCTGGAGA CAGGTGTTGG CTCCTTGAGT 540 CACCAACAGC AGGGACCAGA CCGGGAGGTG TTTCTGGGCG GGAAGGGCTG GGCCAGGCCA 600 GGCTCCAGCA GGCCCCCTTG TGGTCAGAGG GGTTGCCTGC AGGATGATCG GCTTGGGAAC 660 CAAGGCAGCC ACTCCCCACA TGGGAGTTGG ACCCAGGCTT GAAGGACACA TTGTCACATC 720 GATTCACTCT CCTGGGAGGC CTCCTTGTCA CACAAGATGT CCTGGCCCCG GTGTTTTTCT 780 TCACCATATT TCTCCCAACT GTAATTGTGT AGTTCCTGGG GCGCTTATCT CTCAACGTCC 840 ATCTCTGTGA AAAAAGCCGT GACCCTCCAG GATAAGGTCT GTGCGTGAGA CCCCCTGTGT 900 GGAAAGGACG 910
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