Variant report

Variant rs2891159
Chromosome Location chr9:21747672-21747673
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:21743200-21750000 Weak transcription NH-A brain
2 chr9:21743400-21750000 Weak transcription Osteobl bone
3 chr9:21744200-21752200 Enhancers HMEC breast
4 chr9:21745000-21748800 Enhancers NHEK skin
5 chr9:21745800-21747800 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
6 chr9:21746600-21747800 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
7 chr9:21746600-21747800 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
8 chr9:21746600-21748600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
9 chr9:21746600-21748800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
10 chr9:21746600-21751200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr9:21746800-21748400 Enhancers Hela-S3 cervix
12 chr9:21747000-21750000 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
13 chr9:21747200-21752000 Weak transcription Cortex derived primary cultured neurospheres brain
14 chr9:21747600-21750000 Weak transcription NHDF-Ad bronchial

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