Variant report

Variant rs145106727
Chromosome Location chr6:145904944-145904945
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:145904600-145905000 Enhancers H1 Cell Line embryonic stem cell
2 chr6:145904600-145905000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
3 chr6:145904600-145905200 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
4 chr6:145904600-145905400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr6:145904600-145905600 ZNF genes & repeats Lung lung
6 chr6:145904800-145905000 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
7 chr6:145904800-145905200 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
8 chr6:145904800-145905200 ZNF genes & repeats iPS DF 19.11 Cell Line embryonic stem cell
9 chr6:145904800-145905200 ZNF genes & repeats Esophagus oesophagus
10 chr6:145904800-145905200 Enhancers HMEC breast
11 chr6:145904800-145905600 ZNF genes & repeats H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
12 chr6:145904800-145905600 ZNF genes & repeats Foreskin Melanocyte Primary Cells skin01 Skin

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