Variant report

Variant rs1571929
Chromosome Location chr9:101420725-101420726
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:101416600-101420800 Weak transcription NHLF lung
2 chr9:101418200-101421200 Enhancers NHDF-Ad bronchial
3 chr9:101418400-101421200 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
4 chr9:101418600-101420800 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
5 chr9:101419000-101421800 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
6 chr9:101419400-101420800 Weak transcription Adipose Nuclei Adipose
7 chr9:101420400-101421200 Enhancers Fetal Muscle Leg muscle
8 chr9:101420400-101421800 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
9 chr9:101420600-101421000 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
10 chr9:101420600-101421000 Bivalent Enhancer Osteobl bone
11 chr9:101420600-101421200 Enhancers Fetal Stomach stomach
12 chr9:101420600-101421600 Enhancers Fetal Kidney kidney
13 chr9:101420600-101421800 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin

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