Tag | Content |
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EnhancerAtlas ID | HS060-05019 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr11:589240-591380 |
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) |
PRDM1 | MA0508.2 | chr11:591337-591347 | GTGAAAGTGA | - | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr11 | 590142 | 590202 | chr11 | 589256 | 589485 |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I000589 | chr11 | 589256 | 589485 |
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Enhancer Sequence | CATAAGGAGA CGTGTAAGAC ATTTAAAGAG CTTTTCTAAC ACAGCCGTGA CTGAAGCAAG 60 GCCCCTTCCC TTTCGAGACA TCTTGCTCCA TAGAGAGGTT GAGGATGCTG ATTCCGTCCT 120 TCCCAGCAGG AGTTCAGGGT GCTTGATGTG TTGTGAAGTC AACACAGGAG GACAGGAAGG 180 CACCAAGAAT TGCCAAGATA GCTTTGAAAA GGGGAGAAAT TGCCTACTGG ATATTATGAT 240 TTATAAAACT ACAGGGATTG AACTGGAACC GGTCCAGGAA TGGAAACCAG TCCCAGGGGT 300 TTTGCAGGGG CTTAGAAGAG GCCTGGACAC ACTCGGGGGG GCAGGAGGCG CCTGTGGGGC 360 AGGTCAGCTG GGGGCTGCTC ACAGCACACA CACGATGCCG GACGGAGTCA AGATCTCGGA 420 CTAGAAAGCA AAGCTGAACC TTTGAAAAGA AAGCATGGGT AGCTCTGTGA TAAGAAAAGA 480 GAAGGATTTC CTAAACAGTC TGAGAGAGTG TCTGCAAACG GGCACGGAGC ATGTCAGGCT 540 CAGCCTGAGA GGGTGTCTGC AAACGGGCAC AGAGCGTGCG GGGCTCAGCC TGAGAGAGAG 600 TCTGCAAACG GGCACGGAGC GTGCGGGGCT CAGCCTGAGA ATGTCTGCAA ACGGGCATGG 660 AGCGTGCAGG GTTCAGCCTG AGAGGGTGTC TGCAAACGGG CACGGAGCGT GCGGGGCTCA 720 GCCTGAGAGT CTGCAAACGG GCACGGAGCG TGTGGGGCTC AGCCTCAGAG AGTGTCTGTA 780 AACGGGCATG GAGCGTGCGG GGCTCAGCCT GAGAATGTCT GCAAACGGGC ATGGAGCGTG 840 CGGGGCTCAG CCTGAGAATG TGTGCAAACG GGCACGGAGC GTGCAGGGTT CAGCAGCAGG 900 GCTCCTCTGG GAACCCCAGT CCCACCATGG GGGGTGCTGC CGCACACCCC TGGAGCTGGT 960 CGGTAGGAGG GCACCCCAGA CTCCAGAGGT GGGGGTGTCA CACGTACAAC CTCAAAGGCC 1020 ATGTATTCCT GGGTGTTTAC CCAAGAGAAA CAGGAGTGCG CCCACACGAA GACACGTCCA 1080 TCGATGTTCA CCACGGGGGA ATGGACACGT GGACCATTTG TGTGGCAGTG TCTCTTCAGT 1140 GCTAGGGAGG GCAGAATGCC ATGAGCAGAG TCCATGCTGC GGCTCCAATC CTGAGAAACC 1200 CCAGGGAAGA CGTACCTAAC CACACCCCTG AGACAACAGG AAGAAACAGT CAGGTGGGAG 1260 AGGGAAGGGC CCGAAGACCA GGGTGGGTAC TCCACAGGTT GTATATTTGT CAGAGCCGAT 1320 TGAATTATTC AGTTAAAATC AGTGTTTTCT TGTGTATGGT GTACCTTAAT AAAGCCAACA 1380 TAAAGATCTT ATGTGGGTCA GAACACTATT AATAAAGGCA AAAATAAATT TGCAACGTAT 1440 ACCTGACTGT TATCCATACT ATGAAAGTAA ATTTTTTTTT GAGATGGAGT TTGGCTCTTG 1500 TCACCCAAGC TGGAGTGCAG TGGCGCCATC TCGGCTCACC GCAACCTCAG CCTCTCGGGT 1560 TCAAACGATT CTCCTGCCTC AGCCTCCCGA GTAGCTGGGG TTACAGGTAT GCGCCACCAC 1620 ACCTAGCTAA TTTTGTATTT TTAGTAGAGG CGGGGTTTCT CTGTGTCAGT CAGGCTGGTC 1680 TCGAACTCCC GACCTCAGGT AATCTGCCTG CCTCGGCCTC CCAAAGTGCT GGGATTACAG 1740 GTATGAGCCC CTGCTCCCGG CCTATGAAAA GAAATTCTAA AAATTTACTA GTGAATGTCC 1800 AACAATCTTT TGGAAAAGTT AGCAGAAGAC TTGAACAGGC TCGCCGCAGA GGGGCCTGTG 1860 CACAATGCCG CCCCCACGCC TGTCCTTCCT CCCTTTATTG TTCTTACTTG TCACTGAGAT 1920 GCTACGCGTT CATGGAGCTG CTCTTTCCTC CCCGCTAGGG CTGGCAGCTC TGCAGGGAGG 1980 CAAGGCTCGC TGTGCTCCCT CCACTGCCGT GTTGCCAGCA GCTTAGTGGA GGGCCTGGCG 2040 CATGGAGGCA TTTAGCAGAT ACTTGATTTT CAGTGTAAAA GAATTTTTGA TCTCTAAGTG 2100 AAAGTGATTG ACAAGATTCT GATCCTGTTT TTATTTCTCA 2140
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