Tag | Content |
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EnhancerAtlas ID | HS051-05513 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr11:129565220-129566400 |
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 | TCCTCGAGTC CCTCATCAGC CAAAAGAAAA TCATCTCATG AATGCCTACC CTCCAGAAGT 60 GTCACGGGGA GACCATCAGG TGTGTACCAG AAGCACTTCC TACGCTGCAA AGCAGCAAAG 120 AAAGGCAGCC TCTATAGCGG TTTGTAAAGA GTGCCTTGCA GAGAGGACAC AGCCTGGCTG 180 ATGAGTTTCC AGCAGCAGAG CTTTAGGTAT GATTGAATCT TGGAGAGGAA GAGACTTTGG 240 TTCTGTTGAG CCTGCTCCAT GTTTCTCAAA GCACACACCA CCCACTCTGC CAACAGGTAA 300 AGCTTCGGAT GGAACCTGCT GTGTTCTGTC CTCTTCCAGC TGAGCCAGGC CCGCGGGCCC 360 CCTCCAGGAG CTCCGGGCAA GCAGCCCCTC ATGGCCCGTG GTGGAACTGC ACCCTCAGCA 420 CTGGAGAGGG CGGTCGCAGG AGCCTGCGAG GAAGGTGGGG TCTCAGTGCT TTCGCACAGG 480 GCGAGTGGAG CTGGAAATGC AGCCCCCAGT AGTTTCAGTT ATTCCATGTA TGGCTTTTCT 540 CTCTCACCTT GCACCTTTAG ACCCTAATTT CCTGTGAGCA ATGTGCTGGG AAAACTGGCA 600 GCAGCTCTCT GGCAACCCTG GGGGAAAGAA GCGAAGTGGG GTAGAAGCGG AAGCCAGGGG 660 CAGAGGCTGG GTCGGTCCAG CCAGCCCGCG AGGGCTCCCA CGCAGCAGAG GTTCCACTGA 720 GAGGAAGCCG GGGCTGGCCC GGCCGGGAGA CTCCCTCCAC GCCCCGTGTG TGGAGTGCCC 780 GGGCACCCTA TACCCTCAAG GTGGCCTTGA CCTCTGGAGA CAGGTGTTGG CTCCTTGAGT 840 CACCAACAGC AGGGACCAGA CCGGGAGGTG TTTCTGGGCG GGAAGGGCTG GGCCAGGCCA 900 GGCTCCAGCA GGCCCCCTTG TGGTCAGAGG GGTTGCCTGC AGGATGATCG GCTTGGGAAC 960 CAAGGCAGCC ACTCCCCACA TGGGAGTTGG ACCCAGGCTT GAAGGACACA TTGTCACATC 1020 GATTCACTCT CCTGGGAGGC CTCCTTGTCA CACAAGATGT CCTGGCCCCG GTGTTTTTCT 1080 TCACCATATT TCTCCCAACT GTAATTGTGT AGTTCCTGGG GCGCTTATCT CTCAACGTCC 1140 ATCTCTGTGA AAAAAGCCGT GACCCTCCAG GATAAGGTCT 1180
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