Tag | Content |
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EnhancerAtlas ID | HS003-08116 |
Organism | Homo sapiens |
Tissue/cell | A549 |
Coordinate | chr11:64683270-64684430 |
Target genes | Number: 42 | Name | Ensembl ID |
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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: 1 | Chromosome | Start | End |
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Enhancer Sequence | TCCTGTCTCT ATAAAAATAA AAAAGGGGCA GCCTAGAGAC GGCCTTAGAG GCTGAGGCTA 60 AGGTTAGAGG TCAGAGAGGG CTTCCTACAC CAGAATTCAC AGACAGCAGG CCACTGGGGG 120 GTGCCCCCAG TTCAGGGCCC ACGATTATCC TACCCCACAT TTGCTCACCA GGGCCTGGCC 180 TACCCCCAAA GCCTAGCTCT TCTGCCCAGA TTAGCAGCCC CCTGAGTCCA GCCACAAAAC 240 TGAGAAGTCC CTGCCTCCAT GCCCACCCCT GCTGCTCTGG ACCTGGTGGA TCGACCAGGA 300 CGCGCCTCTA ATTGGTGGCT CCTTCAAAGC TCCCCAGGTC AGCTGAGCTG TGAGTCAGGG 360 CTCCTCACCG TTCCCAGCCT CAAGCCTCTG ACCTTACACC TCTTGGCCTC CCTAGCATCT 420 CCCTTGGCCT CCTCCCGGCT TGAAGCCAGA TCTCCCCACC TTTCCTCCAG GGCCTCCCTC 480 CAGGCAGGGA CACTGAGCCG GGGGGGTCGG TGGGAGATGT AGGTGGGGGC CATCCAGTCC 540 CTCCCTAGAC ACCCACTTGG CCCATCCCAC TCTCCCAAAA GCAGGAAGTA GGCAGCGACC 600 CAGGCACACG AGGTGTTGAT CAACACTGGT ACTGACGTAC TGACGCGGTT GTTGACATAC 660 ACATCCGGTG GTTTGTTGAT CCCACCTACG GGCTCAGGAC CGTGGGGTCA AGAGGTCAGG 720 GCACATGATC CACAGGTGTC CTCGCCAGGG CTCCGGACCC CTACCAGCTT CCCCCACCAG 780 CTGCGCAGGC CCAAGTCTGT CACTGCCCTG GCCCAGCTCA GTTCCTACGC TCCCTCCCCA 840 GCCCCTCCTC AGCCCGAGAG CCAACCTCCT TAACTCAGCC CCCAAACTCG ACGAGTTTGT 900 CTTGCATTCT CCAGACAGGT GATCTTGCCC TCTCCAGCCT CAGTTTCTCC TCCCGTGGAG 960 ACAGAAACCC CTTCCCGCTC AGTTTCTGGC TCTGGTAAGG AACTGAAGAG GCCAGCCGGG 1020 GTGCCTCTGA CGCCTGGAGA GGGCAAGATT CCCCTGGCCT CTCTACGCCC GGTGCCTGAT 1080 CCCCCAGCCC GATCCTGCCG CAGGGAGCCT CAGGTCGCTG CGCTCCCACC CTCCGCACCT 1140 TCCTGGACTC GGGCCTGGCT 1160
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