Variant report

Variant rs73421030
Chromosome Location chr9:18509530-18509531
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:18495400-18513200 Weak transcription HUVEC blood vessel
2 chr9:18501600-18510800 Strong transcription HSMM muscle
3 chr9:18501600-18520400 Weak transcription Fetal Stomach stomach
4 chr9:18502200-18518800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
5 chr9:18502800-18520400 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
6 chr9:18506800-18519800 Weak transcription Muscle Satellite Cultured Cells --
7 chr9:18508600-18511000 Weak transcription Osteobl bone
8 chr9:18509400-18509600 ZNF genes & repeats NHDF-Ad bronchial
9 chr9:18509400-18509800 ZNF genes & repeats NH-A brain
10 chr9:18509400-18510000 ZNF genes & repeats Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
11 chr9:18509400-18510600 ZNF genes & repeats Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived

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