Variant report

Variant rs61212477
Chromosome Location chr9:18580203-18580204
allele A/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 chr9:18575000-18581000 Weak transcription NHDF-Ad bronchial
7 chr9:18575400-18581600 Weak transcription NH-A brain
8 chr9:18578800-18582000 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
9 chr9:18579600-18580600 Genic enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
10 chr9:18579600-18581400 Genic enhancers HSMM muscle
11 chr9:18579600-18581400 Enhancers Osteobl bone
12 chr9:18579600-18581600 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
13 chr9:18580000-18580400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
14 chr9:18580000-18581400 Enhancers Muscle Satellite Cultured Cells --
15 chr9:18580200-18581200 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived

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