Tag | Content |
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EnhancerAtlas ID | HS184-18299 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr20:45593950-45594810 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_27008 | chr20:45591273-45595273 | Esophagus | SE_33657 | chr20:45590873-45604189 | H2171 | SE_33856 | chr20:45591109-45594233 | HCC1954 | SE_66991 | chr20:45590873-45604189 | H2171 |
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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 |
GH20I046965 | chr20 | 45594321 | 45594470 |
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Enhancer Sequence | AACAGTCAAG TTAGGTTTTT CTCTGGCTCT TCGAATCCTT AATCCCTTCT CTCCATGTCT 60 GCCCACCAGC AGTGTTCCCA AGTTAGAGCT TCCAGCCCAG GCAGGCCGCC AGAGTCACCA 120 GGCACCCCAG GGCACAGAGA CCCATCCACA GCCTTGGGCA AAGGTGGGGG GTTGGAGGGA 180 AGCCTCTGAG AGAGCTGGAA GGTCCCAGCC CCGCAGTGGC CACCAGGTGC CAGGGCCTGG 240 GCCTCACGCC TCATAGCTCC TGAGTCTGAC CTAAGCGTGC CTTCTTCCCA GCGTGCAGAA 300 CTGTTTGCCT GGGCGTAGGT TGGAGACAGG TGACCCCACC TGGTTGGTTC AGGCCCACGC 360 TTGTTCAGCC TCCTAGACGC TCTGAGTCTT GGCCTCCTGA CTCCTCTGGG GTTGGCGCAG 420 CCTTGCTTGC CTTGGCTCCC GTCCGCCGGG CTGTTCCCTG CACGTACGAG TGGCCCTTTA 480 GAATGTGTTT GTCTGGTCAA GGTTGACAAA CTTCCTGAGC CCACGTCTGT TGACTTTTGT 540 GGGACCTTCT GGCTACCTGG CTGTCGCGGA TGCTTCGCTC AAGCCCTGTC TTCTCTCTTG 600 GGGTGTGGAG TCAGCTAAGA GGGCAGCAGA GCTGGCTGTG TTCACGGAAT CCAGTGTCTG 660 GAGAGAAAGC TGGTGCCCAT GGCGGCTGGG ACTGGCAAGT GAAAACTTGA AATTCCATGA 720 ATGTAGCACC TGGTGATTCT TTGGAGAACT TTAAAATGCA GCATGAGTAT AAACTGTTCT 780 TAACAACCAG GATATGAACG AGGCAACCTC TTACAGTCTT TTTTTCTTTT TCTTTTTTGG 840 GATGGGATAT CCCTCTGTTA 860
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