Tag | Content |
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EnhancerAtlas ID | HS062-14627 |
Organism | Homo sapiens |
Tissue/cell | GM18486 |
Coordinate | chr6:160940830-160942280 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr6:160941058-160941077 | AGGCCGGCAGGGGGCAGCA | + | 6.33 | REST | MA0138.2 | chr6:160941527-160941548 | GCTGCTGGCCCGGGTGCTAAG | - | 6.16 |
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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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| Number: 1 | ID | Chromosome | Start | End |
GH06I160519 | chr6 | 160940433 | 160942270 |
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Enhancer Sequence | CCTAGGGTAG GGTAATGCCA GCGACGGCAG GAAATAGCTC TGACGCACTT AAGAGTTAAA 60 TACAACCTAC AGAAGTTCTG GCTGGGTGGG GAAAACCTAT TGCTAAAGAG AAGAGCTACT 120 TTTTTTCTTT TCTGGAATTT GCAAACAGCA TTTATTCTCA GCCTTACCTT CCACAAGCTC 180 CACCTGGAAC ATTGCTGGGC AGCGTGGAAA CAGAAGCAAA CATCAGCCAG GCCGGCAGGG 240 GGCAGCAGAC CCCACATTTT GCCCTCGCCT CCCGTGGGAG GGAGTGCCCG GCTCCCAAAA 300 TCCTGTGGCG GGTTTTGTCC CAAGCGACTT CAGCCAGCAG ATAGTTCGTG TCCTTCTGAG 360 GCCGCAAAAT TTGGGGTGGA AGAAGTGGGG CGTGAGGCTG AGAGTGAGGA GAGCAATCCA 420 GGGTCGCCAG GGTGGGAGCC GCAGCGGGCC CTAGGCCTCC GGGAGGACAC TGATGCTTCC 480 GGACCGCGCG AGGCGCGCCG GCAATGCCGG CAATGGACGT GCGACAGCGG CACGAGGCGG 540 GGCACCGGGA GGGGATGCGG GGGGAGGGGG GACTCGGGCA TGGCGGGCTT CAGGTTCCGA 600 GCCCTATCCC TGCGGGGAGG CGGCTGAGGC CCAGCGAGAA TTCGAGCGCG GTGCGGGCGG 660 GCCGGCAGTG CTGGGGGGAC CCGGCGCACC CTCTGCAGCT GCTGGCCCGG GTGCTAAGCC 720 CCTCACTGCC AGGAGCCTGC GGCGCCTGCT GGCTGCTTTG AGTGCGGGGC CCGCTGAGTC 780 CGCGCACACC CGGAACTCGC GCTGGCCCGC GAGCGCCGCT CGCAGCACCG GCTCCCGCCC 840 GCGCCTCTCG CTCCACACCT CCCCGCAAGC AGAGGGAGCC GGCTTCCGCC TCGGCCAGCC 900 CAGAGAGGGG CCCGCCACAG CGCAGTGGTG GGCTGAAGGG CTCTTAGAGC ATGGCCAGAG 960 TGGACGCCAA GGCCGAGGAG GCGCCCAGAG TGAGCGAGGG CTGCTAGCAC TTTGTCACCT 1020 CTCAATTTGA CGTTGTAAGC TTCCTTCCAC AGAGTGACCT TTTTCATGCA ATCGATGTGC 1080 TCCTGTGTCA GCTATGCAAA ATAATTTTTG TTTACTGAAT CTGGTTTAAA AGGCAAGAAG 1140 TTGCTTCCCA TTGGGCACTT TGATCCTGGT GAAACGGGAT GTGTATGCCT GGAAACATGG 1200 ACAGTCACAT GCACTGCTTG GTTTTGTGTG GAACTAACAT GAGATGATCT TTTCACTGAT 1260 TTTCAGAATT GTGGAGAATT CACTTAGGAA AATAAGCATG TGTATCAATG CATGACCAAT 1320 ATGGGCGTTT ACTTTAACTG ATTTCACAGA AGCAGTGCTC CTAATATTTT GAGCCACACA 1380 GATTTTATCT GGTGCCTCTT TATGATATGA TCAATTAGCT GCTTACTTCA TAAGTTATGT 1440 GGAGTGGGGA 1450
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