Tag | Content |
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EnhancerAtlas ID | HS147-37513 |
Organism | Homo sapiens |
Tissue/cell | NHEK |
Coordinate | chr6:170653700-170654640 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr6:170654419-170654430 | GGTGACTCATG | + | 6.62 | JUN(var.2) | MA0489.1 | chr6:170654148-170654162 | GTGAGTCATTTCCC | - | 6 | JUND | MA0491.1 | chr6:170654419-170654430 | GGTGACTCATG | + | 6.02 | NKX2-5 | MA0063.2 | chr6:170654468-170654478 | ACCACTTGAG | + | 6.02 | SPI1 | MA0080.4 | chr6:170653958-170653972 | AACTTCCCCTTTTC | - | 6.82 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr6 | 170653802 | 170654490 | chr6 | 170654095 | 170654292 |
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| Number: 1 | ID | Chromosome | Start | End |
GH06I170344 | chr6 | 170653633 | 170655011 |
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Enhancer Sequence | CTATTGCAGT GGATGTCCCC GCCACCACCT GGGCAAGTCC GTAGATCTGG AGTCCCAGTC 60 ACCTCAGCAT GCTTCCCCTA ATCGTTGCGT GGATCCATTC CCTCACCTCT TTGCCTGCCT 120 CTTGTTTTTC CCTTTACATT CCCCCAGTCA GCTTCCCACT GCTGCCAGAG TCCTCCTGCA 180 TAGCAGACTT GATGCTGGTC TTCCTTAGGG CTTCCCTCCA GTGTGCTCCT ATTGCACTTG 240 GGACATTTCC CTTCCCTGAA CTTCCCCTTT TCTTCTCTCG TCTTTGTTCA TTTCTACCCC 300 CTCTTCAAAT CTCAGCTCAA GTCTCTTCCT CACAATGTCT CTGCCCTGCA GCAGCAGTCC 360 TCTGCCCTAC GCTTTGTAGT TGGACACGAG TGTATTTGGT TAGTTTCAGT GTGCTCCACT 420 GATTGTAAAT GTTCCCCGGG GGCAGACAGT GAGTCATTTC CCTGTGTCAG CACCTCCTGT 480 GGTGCCTGGC ATGTGATTGG TTGGATGCTT GGGTAGAGGT CAGGAAGGCT GGAAGGCTTT 540 TATCACTGTC CATTGTTGCC TCCTTTCAAT CCCAGAATAA GTTTTGTTTA TAAGTGTCCT 600 TTATCCAGCA AAGTCCAGCC CAATGTTCCC ACCAGTCTCT TCCATGAAAA TTTATTAATG 660 CCCTGCCCCA ATTTGTTTGT TACTCTCTTT GACCTTCAGA ACTCTAACAG GCTGGGCACG 720 GTGACTCATG CCTATAATCC CAGCTCTTTG GGAGGCCTAG GTGGGAGGAC CACTTGAGGC 780 CAGGTGTTCA AGACCAGCCT GGGCAACATA GCAAGACACT GTCTCCAAAA AAAGGGAAAG 840 AACTCCTGTC ATAAAACCTT CGCACTCTTG TAATATTTGC ACAGCCTTCT CCTGCAAGCT 900 CTTCCAAGGT AGCTAGCAGC TGTTCATCTT TCATGTGGGG 940
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