Tag | Content |
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EnhancerAtlas ID | HS184-26132 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr6:34512480-34513390 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_33601 | chr6:34510887-34516413 | H2171 | SE_41616 | chr6:34512161-34513595 | LNCaP |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH06I034544 | chr6 | 34512443 | 34513350 |
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Enhancer Sequence | CGCTCCCTCA ATCCCCAAGG AAGCCAGGCT GGCTGGGAGC AGCAAAGCTC CACACATGTA 60 CTGTGCTTAA AACAGCCTTC TGAGGTTCCT GACCTCATTC AGCCCTCACA ATGGAAGGCA 120 TGATTGCGCC ATTTGGCGGA TGAGCAAACT GAGGTGGGAA CAAGGGGCCC TCAGTGTCCA 180 AATCTTTCCT GATATAGCAA AGCTTGTTTT TCTTCTGCCT TTGACAAGGA TAGGAGTGGA 240 AGTGGCAGGC AGAGGCCACC ATCCTAAAGG TGGCTATCAT CTTCACCAGC AGGGGAAAGA 300 CGAGAGGAAC AAGGCGGGGT AGAAACCCTC CCACACGCCG GGGAGTAGGC CAGCCCTTGC 360 CCTCCCACAG GGCTATCTGG GGGATCTAAG TAAACTCAAC ACTCTCAAGG TGGCCACTGA 420 GCAAGAGCTC ACAGGTGTGT GTCTCCCAAT ACCCCAGGCT GGGTGCATGG TACCCACCTC 480 CCCTTACCCT CCCTCAGAAG GTGCTGCCCC CAGGGCCCCT TCCAGCTCCC AGTGCTCTCT 540 ACTTTCCCCG ATGCCTGGAG GAGCATGCGG CCACCCGGAG GCAGTGCCAC ATGCCAGGCT 600 TTCCAGGAGG AGCCAGGGTG GTTGTGAGAT GGGGCAGGGC TCCAGGGAAC ACCTAAAACC 660 CTTAGCAACT CAGCCACCTG CTCCTCACTG CTGCCCCAAG GCCCTCCGGG GGAACCATCT 720 GGCCTCAACA CAAGCAGTCA GAGGCCTTGC TCCCCACGGG CCGCCCCGGC TTGGTTTTGC 780 CCAGGCCCTT TTCCCTGAAA CCAATAGCAG AGTGCACAGT TTGGGTGAGA AGGGGGACTG 840 GAGAGGTGCG CAAGCACTGA AACCCCAGGA CATTCTGGGA TGGCAGTGAT GTGGGGGCCT 900 GAGACTTAAG 910
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