Tag | Content |
---|
EnhancerAtlas ID | HS184-15847 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr2:1775420-1777200 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_49937 | chr2:1774587-1777372 | RPMI-8402 |
|
| 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 |
GH02I001772 | chr2 | 1776761 | 1776910 |
|
Enhancer Sequence | AGAGGCTTCT GTAGCCATTA AACAGATTTA CATACATTAG AAAAAGAAAG AAAGAAAGAA 60 TATCTGTAGG GAAAGGGAAA GAGGAAGGAT CTTATCTTCA GTAATAAGAA TGCAGCCTCT 120 CACTGTATTT GTCCTGGCAC TGGGAGCTGG TTAGGGTGCA TGTTCCCAGG CTGCACCCCA 180 GAGGCCCCTG GATAGAATCT GCAGGAAGAG GGTGGCCACT GTTCACACGA GGCACCTCCT 240 GCCTCTGGTC CTTTCTACAG CAGCAGTGGA ACTCTGGTCT CAGGTGGAAT GCACTGGACC 300 CTCCCTAGCA CTGGGTACAA CTCTGGTATT GGGTGGAACA CACTAGACCC TCCCTTGTAC 360 TGGTGGAACT CTGGTCTTGG GTGGAATGCA CTGGACCCTC CCTTCTTGCT GCCCCTGAGG 420 AATGTTCTGG GATGAACCAC AAGTGGGGAC CATAGAGGGC ACCTGACAGA GGGGTGCTCG 480 GTGTCACCAG GATCCCAAGG GCCTGACGTT GGAGCCAAGG GCAGTGCATG TAAAGAGGCC 540 TAAGTGAATG GCTGGCCCCC AGCCTCTGTG AGTGTCAGGC TCCTGGGCTC TTATGTGTCA 600 GTGTTTCATC AAATTTGTAT TGGCCTCTCA TCAGATCAGC CCAAGGATCC ACGTTCCAGG 660 CCATTTCTGC AGCAGTTAGC ATGTCTCACA GTGGGGTTTC TCTGCTTGCT CCTTAAGCCT 720 TGCTTTTTCA GGCTTGCCCT CAGAGTGGCC ATTAGCCCTG ATTGTTTCAG GACCCCAAGG 780 CTGGGCCCAT CTCTACCCAG AGCACACCAG AACGAGGGCA CCCAGCAGTG GATTCACAAA 840 CACAACTGAG CTCCCAGCTT CCAGTTCCTT ACACTGGGAT TTCTTACTGT GCCAAGCAAT 900 GTTATAAATG AACAGAGGCC TGTGGGCTTA ACTCTCAGAG CTTCTCCTGG AGAGCAGCAC 960 TGCTTGTCAG AGCAGCCCCT CTAAGCCTCA GGAGGCCAGT GCCCTTTTCC ATTGGCCCAT 1020 TGCCACTCTG CTCTTAAATC CACATAAGCA TATCCTAAGT TAAAAAAAAA TGCAATTTGC 1080 CAATTATTCG ATGAGTGGCA GGTCTCAGGA AGAGCTTGCC TGGTACACAA TTTGCACCAG 1140 GAAGTGGAGG CTGCATTAAG GACAAGGGCT GGAGGCCATC TCTCCAACCG GAGGACCAAA 1200 GCTGAGAGGA GAGGAAGCAT CAGGTGGGGC TCAGAAACTG AACCCTGCCC TTCATCAGAA 1260 AATACGAGAT CAAGATTCAA GTCCAGACTG AAGGACGACT TTCCAGGCCT GAAGAGCGAA 1320 GGGACCCTCT GCTTGGGCTG CGCTGAAAGA ATTTTAAAAA TGTGACTGCA GGCTAATCCT 1380 TCCAACTTTC CATCAGATAA GCCTAAAGCA TTTAAGAACA TTTTTGAACC AACAGTTCAT 1440 TAAATTCCAG GACATATTTT GAGCACTACA GCAAATAATG ACACGTAATT CACAAGCAAC 1500 AGGCAAGTGG AGGCTCTAAG CTGAATGGCC CAGGGACCCT CCAGCCATGA ACATCCAACA 1560 AGAAGCCTCA TGTACTTTGT AACTGGCTAA GCTGCTCATA ACAACGCTGG AAACATGTGG 1620 AAAGAGATCA GGGTGCGAAG GCATTGCATA GAGACGCCCA GGAGAGTGGG AAGAGTCCCC 1680 AGAAGTTAGC GCCAGCAGGG CGGCCTCCAG GAGGGCAGGC AACACCTGCA AAGATTCGTC 1740 ACCTGATGCT CTAGATCCTT CTGAGGCCAA CCCATCAGCT 1780
|