Variant report

Variant rs11670942
Chromosome Location chr19:43652526-43652527
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:43650800-43654600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
2 chr19:43650800-43655400 Enhancers NHEK skin
3 chr19:43651400-43654400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
4 chr19:43651600-43654400 Enhancers HMEC breast
5 chr19:43651800-43652800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr19:43651800-43653000 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
7 chr19:43651800-43653800 Enhancers NHDF-Ad bronchial
8 chr19:43652000-43652600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
9 chr19:43652000-43653000 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
10 chr19:43652200-43653200 Enhancers Muscle Satellite Cultured Cells --
11 chr19:43652200-43653200 Enhancers Osteobl bone
12 chr19:43652200-43655200 Weak transcription Esophagus oesophagus
13 chr19:43652400-43652800 Enhancers Placenta Amnion Placenta Amnion

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