Variant report

Variant rs3849929
Chromosome Location chr9:21769412-21769413
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:21762600-21770200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr9:21765400-21770400 Weak transcription NHLF lung
3 chr9:21765400-21770600 Weak transcription Muscle Satellite Cultured Cells --
4 chr9:21765400-21770600 Weak transcription NH-A brain
5 chr9:21765400-21770600 Weak transcription Osteobl bone
6 chr9:21765400-21772600 Weak transcription HSMM muscle
7 chr9:21765600-21770200 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
8 chr9:21765600-21770400 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
9 chr9:21765600-21770600 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
10 chr9:21765600-21770600 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
11 chr9:21765600-21770600 Weak transcription NHDF-Ad bronchial
12 chr9:21765600-21770800 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
13 chr9:21767200-21771000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
14 chr9:21769200-21770400 Weak transcription Stomach Mucosa stomach

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