Tag | Content |
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EnhancerAtlas ID | HS060-06044 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr11:64682780-64684430 |
Target genes | Number: 38 | Name | Ensembl ID |
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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) |
Nr2f6(var.2) | MA0728.1 | chr11:64683973-64683988 | GGGGTCAAGAGGTCA | + | 8.07 | Nr2f6 | MA0677.1 | chr11:64683329-64683343 | AAGGTTAGAGGTCA | + | 6.06 | RARA | MA0729.1 | chr11:64683973-64683991 | GGGGTCAAGAGGTCAGGG | + | 6.56 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr11 | 64682870 | 64682981 | chr11 | 64682863 | 64683400 | chr11 | 64683400 | 64683600 |
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Enhancer Sequence | GGGCCTCAGT AAACTGGTTG GATCCAAGAA TAAAAAAGCA CATGGCAGAG CAGATGGGAG 60 TCCAAATTCC TCACCCAGAG ACCCACAGCT CGGGAAACTG AGGCCTAGAG ACAGGACTAA 120 TCTAGTCACC CAGTATACAA CAGGGACTGA GACTGGGATG CGGGCCTCTT TCTTTTCATG 180 CCACTTCAGA GGCCCCAGAT ACTCAGTTTC TTTGGGGGCC TTCAAGGCGG GGCCTGCAGG 240 CTGAGCTGGG AGGGAGGAGG GGCTGGTTAT CAAGAAAGCG CCTGCATTCC ACCAGGGCCC 300 TAGAGAAGCC AATTCAATCC CCAACAAGAG GGCAGGGAAC AGGAGTAGGG GCGTTTTCTG 360 GAGCTGAAAG TAAAAAGGGG AAGCCTAGGG CTGGGTATGG TGGTTCATGC CTATAATCTC 420 AGCACTTTGG GAGGCTGAGG TGGGAGGATC CCTTCAGGGG TTCAAGGCTA GCCTGGGCAA 480 CATAGCGAAA TCCTGTCTCT ATAAAAATAA AAAAGGGGCA GCCTAGAGAC GGCCTTAGAG 540 GCTGAGGCTA AGGTTAGAGG TCAGAGAGGG CTTCCTACAC CAGAATTCAC AGACAGCAGG 600 CCACTGGGGG GTGCCCCCAG TTCAGGGCCC ACGATTATCC TACCCCACAT TTGCTCACCA 660 GGGCCTGGCC TACCCCCAAA GCCTAGCTCT TCTGCCCAGA TTAGCAGCCC CCTGAGTCCA 720 GCCACAAAAC TGAGAAGTCC CTGCCTCCAT GCCCACCCCT GCTGCTCTGG ACCTGGTGGA 780 TCGACCAGGA CGCGCCTCTA ATTGGTGGCT CCTTCAAAGC TCCCCAGGTC AGCTGAGCTG 840 TGAGTCAGGG CTCCTCACCG TTCCCAGCCT CAAGCCTCTG ACCTTACACC TCTTGGCCTC 900 CCTAGCATCT CCCTTGGCCT CCTCCCGGCT TGAAGCCAGA TCTCCCCACC TTTCCTCCAG 960 GGCCTCCCTC CAGGCAGGGA CACTGAGCCG GGGGGGTCGG TGGGAGATGT AGGTGGGGGC 1020 CATCCAGTCC CTCCCTAGAC ACCCACTTGG CCCATCCCAC TCTCCCAAAA GCAGGAAGTA 1080 GGCAGCGACC CAGGCACACG AGGTGTTGAT CAACACTGGT ACTGACGTAC TGACGCGGTT 1140 GTTGACATAC ACATCCGGTG GTTTGTTGAT CCCACCTACG GGCTCAGGAC CGTGGGGTCA 1200 AGAGGTCAGG GCACATGATC CACAGGTGTC CTCGCCAGGG CTCCGGACCC CTACCAGCTT 1260 CCCCCACCAG CTGCGCAGGC CCAAGTCTGT CACTGCCCTG GCCCAGCTCA GTTCCTACGC 1320 TCCCTCCCCA GCCCCTCCTC AGCCCGAGAG CCAACCTCCT TAACTCAGCC CCCAAACTCG 1380 ACGAGTTTGT CTTGCATTCT CCAGACAGGT GATCTTGCCC TCTCCAGCCT CAGTTTCTCC 1440 TCCCGTGGAG ACAGAAACCC CTTCCCGCTC AGTTTCTGGC TCTGGTAAGG AACTGAAGAG 1500 GCCAGCCGGG GTGCCTCTGA CGCCTGGAGA GGGCAAGATT CCCCTGGCCT CTCTACGCCC 1560 GGTGCCTGAT CCCCCAGCCC GATCCTGCCG CAGGGAGCCT CAGGTCGCTG CGCTCCCACC 1620 CTCCGCACCT TCCTGGACTC GGGCCTGGCT 1650
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