Variant report

Variant rs7044968
Chromosome Location chr9:18581204-18581205
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:18564400-18591800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr9:18569800-18601000 Weak transcription NHLF lung
3 chr9:18570200-18583200 Weak transcription Fetal Stomach stomach
4 chr9:18570200-18591800 Weak transcription Aorta Aorta
5 chr9:18574400-18581600 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
6 chr9:18575400-18581600 Weak transcription NH-A brain
7 chr9:18578800-18582000 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
8 chr9:18579600-18581400 Genic enhancers HSMM muscle
9 chr9:18579600-18581400 Enhancers Osteobl bone
10 chr9:18579600-18581600 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
11 chr9:18580000-18581400 Enhancers Muscle Satellite Cultured Cells --
12 chr9:18580400-18585400 Weak transcription Rectal Smooth Muscle rectum
13 chr9:18580600-18586800 Strong transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
14 chr9:18581000-18582600 Strong transcription NHDF-Ad bronchial
15 chr9:18581200-18588400 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived

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