Variant report

Variant rs60199560
Chromosome Location chr9:18507009-18507010
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:18490400-18509400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr9:18495400-18513200 Weak transcription HUVEC blood vessel
3 chr9:18501600-18510800 Strong transcription HSMM muscle
4 chr9:18501600-18520400 Weak transcription Fetal Stomach stomach
5 chr9:18502200-18518800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
6 chr9:18502600-18509400 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
7 chr9:18502800-18507200 Weak transcription ES-I3 Cell Line embryonic stem cell
8 chr9:18502800-18520400 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
9 chr9:18504000-18508600 Strong transcription Osteobl bone
10 chr9:18504200-18508000 Strong transcription NHDF-Ad bronchial
11 chr9:18504400-18509400 Strong transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
12 chr9:18504800-18508600 Strong transcription NH-A brain
13 chr9:18505400-18507400 Weak transcription HUES64 Cell Line embryonic stem cell
14 chr9:18505400-18507400 Weak transcription iPS-15b Cell Line embryonic stem cell
15 chr9:18505600-18507400 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
16 chr9:18506800-18519800 Weak transcription Muscle Satellite Cultured Cells --

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