Variant report

Variant rs12336889
Chromosome Location chr9:110746215-110746216
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:110741000-110747200 Enhancers Primary monocytes fromperipheralblood blood
2 chr9:110744200-110747200 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
3 chr9:110744600-110746400 Enhancers Muscle Satellite Cultured Cells --
4 chr9:110744600-110746400 Enhancers NHEK skin
5 chr9:110745000-110746400 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
6 chr9:110745000-110746400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr9:110746000-110751200 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
8 chr9:110746200-110746400 Active TSS Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
9 chr9:110746200-110747000 Enhancers Monocytes-CD14+_RO01746 blood
10 chr9:110746200-110750000 Weak transcription Primary neutrophils fromperipheralblood blood
11 chr9:110746200-110751200 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
12 chr9:110746200-110751200 Weak transcription NHDF-Ad bronchial

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