Tag | Content |
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EnhancerAtlas ID | HS183-01986 |
Organism | Homo sapiens |
Tissue/cell | T47D-MTVL |
Coordinate | chr17:25567000-25569400 |
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) |
SOX10 | MA0442.2 | chr17:25567103-25567114 | GTCTTTGTTTT | - | 6.14 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr17 | 25567080 | 25567246 | chr17 | 25567255 | 25567397 | chr17 | 25568367 | 25569018 |
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| Number: 1 | ID | Chromosome | Start | End |
GH17I027237 | chr17 | 25564882 | 25573648 |
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Enhancer Sequence | AACGGGTCCA CCTCTTCGCC CTTTCCCTTT CTTGTTTGTC TTCCTCCCTT CCTCGTTTGA 60 TCATTCTCTG TCTGCTTCCC CCACTAGAAT AAAGACCTGT GGGGTCTTTG TTTTGTGCAT 120 GGCTGTATCT TTAGGATCTA GGAGAAGGTG CTCCCTCACT ATTAATTCAA CAAACCAGTG 180 AATGAATGAG TGGCCGCCAG GATTAGCGGG GCTGGTGGGC AGAGCAGAAG CAGTCTGGAT 240 GCCGAGATTT GAGGGAAAGC TCCCTCCAAG CCCTCAGGAC TCACTGTAGG GTTAACTCAC 300 TGTAGGGTTA ACAGGGCCCA GCTCTGGCAG AGCACAGTTC AACAGCCAGG AATGAGCTCA 360 GCTCCCGTCC CCACTCCCCC CTTCATCAGA AGACTGAGCA GCTTTTTCCC TCTGCCAGGC 420 TTCCAGCAAT ACCTCCCCTT GGGGTCTTTT CTGCTTATTC TCCCTTGGGA GGTACTGTGG 480 GAGTCCAGGG ATTGGGGTGG GGTGCAAGCG TGAGGGTCTC TGGGGAAGGG AGACTGTAAA 540 CACTTCCATT TTAGCACTGA AATCCCTGAA GTCTCTTCCC TCTGGCTGGT TGGTTCAGCC 600 AGAATAAACT TTCTTTTGGG GTGAGCAGCT TGGCTGGCTT TTCAAGACTC AGTTCAGACA 660 TCTTTGCCGC CCGTCTTCCA GGTTAGTGCC CTCTTTGCTG TCCTCAGGAT GGTCTCAGCC 720 CTCTCTCTGC TTCTCACAGC AGCGTTGCCT CTGTCTGCTT CTCAGAGAAC ACTCACGGTC 780 TGGGGTCGTG CCTTTCTTCC TCTGGGCCCC AGGCCCAGAA TGGCAGGGGC TCAAATCAAT 840 GTTTGTTGAG TAAATGAAGT GGGATGGGGA GGCGACCGAT GTTACCATCT GAGAGCCAGC 900 ACTGTGCATC ATCAATGTTT GCATGCCTTC TCCAGCTACA AGTGCCAGGG TCAGCCGCGA 960 ATCCAGAGGG GACCACATTT TATGTAGGCC ATAGGACTGA CTCAAGACAA ATAATGCTTT 1020 GCCCTGCAAA ATCAGTGCTG TTGGGCCAGG AGTGGTGGCT CACACCTGTA ATCCCAACAC 1080 TTTTGGAGGA CGAGATGGGT GGAACACCTG AGGTCAGGAG TCAGAGACCA GCCTGGCCAA 1140 CATGGTGAAG CTCCATCTCT AACTATAAAT ACAAAAAAAA ATTAGCTGGG CGTGGTGGTG 1200 TGTGCCTGTA ATCCCAGCTA CTAAGGGGGG CTGAGGCAGG AGAATTGCTT GAACCTGGGA 1260 GGCAGAGGTT GCAGTGAGCC AAGATCGCAC CACTGCACTC CAGCCTGGGC AACGAGACCC 1320 CGTCTCAGAA AAAAAGGAAA AAAAAGAAAA GAAAAACCAG TGTTGCTGGT AGCAGGCTGC 1380 CCCACGGTTA GTCCCTATCC AGCTCAGAGA ATGAAGACAC CAGCATCAGG GGCATCTCCC 1440 TCACTCCTCC CTTCCCTCAA GCTCCAACAG CTTCTTGCAT GCATCCTCCC ACTGACTGCA 1500 GAGTGGAGGG TGGGGAGTGG GGGCAGTTCT CATTTACAGG GGGAAAGAAA TCCTGGGTGG 1560 GGGTGAGAAA GGGGAAGAGC AGTAGGGGAA GCCCTGAGGG TTGGGTGAGC ACCCCTGGAA 1620 GCCCAGAAAC CTCATTACCT TCCATTCTGA CTCATCTGTC TTCTAATTCT TTCTAGCTTC 1680 TTGGCAAGGA CAGAGGACCC TGCTGAGAGG GCTTCAGGAA TGGCCAAAGA CTGAGACGGT 1740 GCAGCCTCAG CCACGCCCAG AAAGAACTTG GATAAGTCTG TCTTGCTGTT TTTCCAGTTT 1800 TTGTTTGCAC CTCACAGGAA GAACTGGTCC GCCTTCATTC CTAGCCCCAC CAAACTGACA 1860 GGTTAGACTG ACTCAGGGAC CATCCCCTTT GTCAGGCAGT TCCCTCACTT GCTGGACTGA 1920 CCGTGGTTCT GCAGTGTGGT TGGGGCCCCT GCATAACACT TTAGCCAACA ACTACATTAG 1980 AGAACTCTTT GTCTAGACTA AAGCCACATT TCCCAAAGTC GTCAGATTAA AGACATCACC 2040 TGGAAGTTCT GATTGGGTCG GTCTGGGGAT GCCCTGAAAT CGACTTCTGA AGCGCGCCAG 2100 ATGATTTATA AAATAGCTCA GTAAAAACCA AGCTCAGCCG GGCACAGTGG CTCACGCCTG 2160 TAATCCCAGC ACTTTCAGGG GCCAAGGTGG CTGGGTCACT TAGGCCCAGG AGTTCAAGAC 2220 CAGCCTGACC AACATGGTGA AACCCCGTCT CTACTAAAAA TACAAAAATT AGCCAGACAT 2280 GGTGGCACAT GCCTGTAATC CCAGCTACTC AGGAGGCTGA GGCAGGAGAA TCAGTTGAAC 2340 CTGTGAGGCA GAGGTTGCAG TGAACTGAGA CCGTGCCATT GCACTCCAGC CTGGGCAACA 2400
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