Variant report

Variant rs340893
Chromosome Location chr9:6097390-6097391
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:6091000-6098200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
2 chr9:6096400-6099400 Enhancers NHEK skin
3 chr9:6096400-6100000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
4 chr9:6096400-6100200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr9:6096400-6100200 Enhancers Fetal Adrenal Gland Adrenal Gland
6 chr9:6096400-6100400 Enhancers HMEC breast
7 chr9:6096600-6097600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
8 chr9:6096600-6099000 Enhancers Osteobl bone
9 chr9:6096600-6099200 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
10 chr9:6096600-6099200 Enhancers NHDF-Ad bronchial
11 chr9:6096600-6100200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
12 chr9:6096800-6098400 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
13 chr9:6097200-6098400 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived

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