Variant report

Variant rs548815748
Chromosome Location chr1:90747889-90747890
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:90736200-90752000 Weak transcription Aorta Aorta
2 chr1:90747200-90748000 Enhancers NHEK skin
3 chr1:90747200-90748400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
4 chr1:90747200-90748600 Enhancers iPS-20b Cell Line embryonic stem cell
5 chr1:90747200-90748800 Enhancers Fetal Lung lung
6 chr1:90747400-90748000 Enhancers Breast Myoepithelial Primary Cells Breast
7 chr1:90747400-90748200 Enhancers HMEC breast
8 chr1:90747800-90748000 Weak transcription HUES48 Cell Line embryonic stem cell
9 chr1:90747800-90748000 Flanking Active TSS Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
10 chr1:90747800-90748000 Flanking Active TSS Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
11 chr1:90747800-90748600 Enhancers H1 Cell Line embryonic stem cell

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