Variant report

Variant rs1889006
Chromosome Location chr9:18617804-18617805
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:18606200-18624400 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
2 chr9:18606600-18632200 Weak transcription NHLF lung
3 chr9:18607200-18622000 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
4 chr9:18607400-18622200 Weak transcription Muscle Satellite Cultured Cells --
5 chr9:18608800-18622000 Weak transcription Osteobl bone
6 chr9:18608800-18622400 Weak transcription NH-A brain
7 chr9:18611400-18622200 Weak transcription Fetal Heart heart
8 chr9:18612000-18630600 Weak transcription Aorta Aorta
9 chr9:18612600-18627600 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
10 chr9:18614800-18618000 Weak transcription Ovary ovary
11 chr9:18616000-18622000 Weak transcription HSMM muscle
12 chr9:18617200-18618200 Enhancers Fetal Stomach stomach
13 chr9:18617800-18618200 Genic enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
14 chr9:18617800-18618800 Strong transcription NHDF-Ad bronchial

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