Variant report

Variant rs3762426
Chromosome Location chr9:17019516-17019517
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:17016600-17020400 Enhancers Cortex derived primary cultured neurospheres brain
2 chr9:17018000-17019800 Enhancers Breast Myoepithelial Primary Cells Breast
3 chr9:17018200-17019800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
4 chr9:17018400-17019600 Enhancers NHEK skin
5 chr9:17018400-17021200 Weak transcription Fetal Thymus thymus
6 chr9:17019200-17019800 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
7 chr9:17019200-17021000 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
8 chr9:17019400-17019800 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
9 chr9:17019400-17020000 Enhancers Stomach Mucosa stomach
10 chr9:17019400-17021200 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
11 chr9:17019400-17021200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
12 chr9:17019400-17022400 Weak transcription Muscle Satellite Cultured Cells --

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