Variant report

Variant rs111898747
Chromosome Location chr9:18519718-18519719
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:18501600-18520400 Weak transcription Fetal Stomach stomach
2 chr9:18502800-18520400 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
3 chr9:18506800-18519800 Weak transcription Muscle Satellite Cultured Cells --
4 chr9:18510600-18533000 Weak transcription NHDF-Ad bronchial
5 chr9:18513800-18520600 Weak transcription NH-A brain
6 chr9:18517400-18519800 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
7 chr9:18519200-18521000 Enhancers Osteobl bone
8 chr9:18519200-18521400 Genic enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
9 chr9:18519400-18533600 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
10 chr9:18519600-18521200 Genic enhancers HSMM muscle
11 chr9:18519600-18521400 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow

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