Tag | Content |
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EnhancerAtlas ID | HS006-07071 |
Organism | Homo sapiens |
Tissue/cell | Astrocyte |
Coordinate | chr11:64682830-64684430 |
Target genes | Number: 27 | 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 | CAGATGGGAG TCCAAATTCC TCACCCAGAG ACCCACAGCT CGGGAAACTG AGGCCTAGAG 60 ACAGGACTAA TCTAGTCACC CAGTATACAA CAGGGACTGA GACTGGGATG CGGGCCTCTT 120 TCTTTTCATG CCACTTCAGA GGCCCCAGAT ACTCAGTTTC TTTGGGGGCC TTCAAGGCGG 180 GGCCTGCAGG CTGAGCTGGG AGGGAGGAGG GGCTGGTTAT CAAGAAAGCG CCTGCATTCC 240 ACCAGGGCCC TAGAGAAGCC AATTCAATCC CCAACAAGAG GGCAGGGAAC AGGAGTAGGG 300 GCGTTTTCTG GAGCTGAAAG TAAAAAGGGG AAGCCTAGGG CTGGGTATGG TGGTTCATGC 360 CTATAATCTC AGCACTTTGG GAGGCTGAGG TGGGAGGATC CCTTCAGGGG TTCAAGGCTA 420 GCCTGGGCAA CATAGCGAAA TCCTGTCTCT ATAAAAATAA AAAAGGGGCA GCCTAGAGAC 480 GGCCTTAGAG GCTGAGGCTA AGGTTAGAGG TCAGAGAGGG CTTCCTACAC CAGAATTCAC 540 AGACAGCAGG CCACTGGGGG GTGCCCCCAG TTCAGGGCCC ACGATTATCC TACCCCACAT 600 TTGCTCACCA GGGCCTGGCC TACCCCCAAA GCCTAGCTCT TCTGCCCAGA TTAGCAGCCC 660 CCTGAGTCCA GCCACAAAAC TGAGAAGTCC CTGCCTCCAT GCCCACCCCT GCTGCTCTGG 720 ACCTGGTGGA TCGACCAGGA CGCGCCTCTA ATTGGTGGCT CCTTCAAAGC TCCCCAGGTC 780 AGCTGAGCTG TGAGTCAGGG CTCCTCACCG TTCCCAGCCT CAAGCCTCTG ACCTTACACC 840 TCTTGGCCTC CCTAGCATCT CCCTTGGCCT CCTCCCGGCT TGAAGCCAGA TCTCCCCACC 900 TTTCCTCCAG GGCCTCCCTC CAGGCAGGGA CACTGAGCCG GGGGGGTCGG TGGGAGATGT 960 AGGTGGGGGC CATCCAGTCC CTCCCTAGAC ACCCACTTGG CCCATCCCAC TCTCCCAAAA 1020 GCAGGAAGTA GGCAGCGACC CAGGCACACG AGGTGTTGAT CAACACTGGT ACTGACGTAC 1080 TGACGCGGTT GTTGACATAC ACATCCGGTG GTTTGTTGAT CCCACCTACG GGCTCAGGAC 1140 CGTGGGGTCA AGAGGTCAGG GCACATGATC CACAGGTGTC CTCGCCAGGG CTCCGGACCC 1200 CTACCAGCTT CCCCCACCAG CTGCGCAGGC CCAAGTCTGT CACTGCCCTG GCCCAGCTCA 1260 GTTCCTACGC TCCCTCCCCA GCCCCTCCTC AGCCCGAGAG CCAACCTCCT TAACTCAGCC 1320 CCCAAACTCG ACGAGTTTGT CTTGCATTCT CCAGACAGGT GATCTTGCCC TCTCCAGCCT 1380 CAGTTTCTCC TCCCGTGGAG ACAGAAACCC CTTCCCGCTC AGTTTCTGGC TCTGGTAAGG 1440 AACTGAAGAG GCCAGCCGGG GTGCCTCTGA CGCCTGGAGA GGGCAAGATT CCCCTGGCCT 1500 CTCTACGCCC GGTGCCTGAT CCCCCAGCCC GATCCTGCCG CAGGGAGCCT CAGGTCGCTG 1560 CGCTCCCACC CTCCGCACCT TCCTGGACTC GGGCCTGGCT 1600
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