Variant report

Variant rs12351319
Chromosome Location chr9:18697066-18697067
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:18675800-18710000 Strong transcription HSMM muscle
2 chr9:18680000-18701600 Strong transcription Osteobl bone
3 chr9:18690000-18714200 Weak transcription HUVEC blood vessel
4 chr9:18693000-18703000 Weak transcription Fetal Heart heart
5 chr9:18695000-18699600 Strong transcription NH-A brain
6 chr9:18695200-18699000 Strong transcription NHDF-Ad bronchial
7 chr9:18695200-18703000 Weak transcription HSMMtube muscle
8 chr9:18695400-18701800 Strong transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
9 chr9:18695400-18706400 Weak transcription NHLF lung
10 chr9:18696000-18697200 Strong transcription Foreskin Fibroblast Primary Cells skin01 Skin
11 chr9:18696400-18702800 Weak transcription Fetal Muscle Trunk muscle
12 chr9:18696400-18702800 Weak transcription Fetal Stomach stomach
13 chr9:18696400-18703200 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
14 chr9:18696400-18704000 Weak transcription Duodenum Smooth Muscle Duodenum
15 chr9:18696400-18705000 Weak transcription Fetal Muscle Leg muscle
16 chr9:18696600-18699800 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
17 chr9:18696600-18705800 Weak transcription Muscle Satellite Cultured Cells --
18 chr9:18696800-18706600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
19 chr9:18697000-18705800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin

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