Variant report

Variant rs544787
Chromosome Location chr9:18694752-18694753
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:18675600-18695000 Weak transcription NHLF lung
2 chr9:18675800-18710000 Strong transcription HSMM muscle
3 chr9:18680000-18701600 Strong transcription Osteobl bone
4 chr9:18687800-18694800 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
5 chr9:18690000-18695000 Strong transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
6 chr9:18690000-18714200 Weak transcription HUVEC blood vessel
7 chr9:18691800-18694800 Weak transcription Aorta Aorta
8 chr9:18693000-18694800 Strong transcription Foreskin Fibroblast Primary Cells skin01 Skin
9 chr9:18693000-18694800 Strong transcription Foreskin Fibroblast Primary Cells skin02 Skin
10 chr9:18693000-18703000 Weak transcription Fetal Heart heart
11 chr9:18693800-18696400 Strong transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
12 chr9:18694000-18695200 Weak transcription NHDF-Ad bronchial
13 chr9:18694200-18695400 ZNF genes & repeats Muscle Satellite Cultured Cells --
14 chr9:18694600-18695000 Weak transcription NH-A brain
15 chr9:18694600-18695200 ZNF genes & repeats HSMMtube muscle
16 chr9:18694600-18696400 ZNF genes & repeats Fetal Stomach stomach
17 chr9:18694600-18696800 ZNF genes & repeats H1 Derived Mesenchymal Stem Cells ES cell derived

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