Tag | Content |
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EnhancerAtlas ID | HS184-18539 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr20:55309840-55311010 |
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) |
RREB1 | MA0073.1 | chr20:55310917-55310937 | CCCCACCCCCACCCCCACCC | + | 6.27 | RREB1 | MA0073.1 | chr20:55310918-55310938 | CCCACCCCCACCCCCACCCC | + | 6.27 | RREB1 | MA0073.1 | chr20:55310923-55310943 | CCCCACCCCCACCCCCACCA | + | 6.27 |
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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: 2 | ID | Chromosome | Start | End |
GH20I056736 | chr20 | 55309773 | 55309850 | GH20I056734 | chr20 | 55309983 | 55310678 |
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Enhancer Sequence | AAACCCAAAA AACTGATGGA GGCACTTTCT TAAGCAGATT GGAGGCCCTG CACCCTGCTA 60 GGGGCTGGGT CCCCACCCTG GAAGCCTATA TTTAGATATC TGAGAGTGAA ACAGGAGGGA 120 AAGAAACAAA ATGAAGAAAA CTTCTGTAAG CCTCAGTTTC CTCGTGCAAA ATGTGGACGT 180 TAATAGTATC TCCTTACCTC GGGGTCACCA CGGTATTGGA TAAAATAATG CCAGTAAAAG 240 GTGTCCCAGT ATCAGAGAAG ATGGCCATTA CTCAAAGGCT TGCTCTAGCA AATGTCAAGC 300 TACAGACAGA AATCAGCGCT CTCAAGGAGA GCTTGAGGGT GAGATTTTGG TCTAGATTTG 360 GGCATGGCAG TGGCAGTCGG GAGAGGCTTC CCTGGGGAGG CAGCCAGGCC TGCAAACGGT 420 GTTTATCGTT CTCTCCATCT GGCATTAGGG CCAGAGCACT ACTGTCTCTC TGTTCCCCCA 480 ACACGACGCG CTGCCAGCAC CCACACTGCT GCAGAGCCTT AGCACAGGCT GCTTGCTCCG 540 CTGGATCACA CCCAAACCAT GGCCTGGCTG GCTCCTTGTT GACTTTCAAT TCTGAGATGA 600 ATGATCATCT CCCTGGAAAA GGCTCTGCCA CTCTCCAATG ACCCAGCTCT GGTTTATCTT 660 CACCGTGCTG ATCGCCCCTG CAATCTGTTT GCTTTCAGCT CTTGGACCTG TTCTTCCCTA 720 CCCACCCAGG TGCGCTTGGT GCTGTGTGCA CAGTAGGTGC TCGGTCAATA TTTGTCCAGG 780 GCATAACACG CCTTCCAGCA GTGTGGCTCC AGCTCCGAGG GCATATTCAT CATCGGGGGA 840 TCTTGTTAGA ATCAAGGGTC CAGTTCAGTA GGTCTGGAGT GGGGCCCAGG AGTCTAAGTG 900 TCTGAGAAGC TTCCAGGTAT TGTGATGCTG CAGGTAGGTG GGCCGTGCTT TGGGGTTCAA 960 GAGTGTGTGA ATGGGACAGC TGCGACCTGG GGCGTCAACA GAGGGAGGGG CTGGTTGAAA 1020 CAGGGAGGGG CTTCATTGAG GAGGAGACCC TGATATTTAA GTAATGGAAT TTGTCTCCCC 1080 CACCCCCACC CCCACCCCCA CCATCCCTTC ATCCCTGCTG CCATTATTTC TCAGCCACGT 1140 TATTTTTTTT TTTTGAGACA CAGTCTCGCT 1170
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