Variant report

Variant rs12376154
Chromosome Location chr9:18588271-18588272
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 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 chr9:18570200-18591800 Weak transcription Aorta Aorta
4 chr9:18581200-18588400 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
5 chr9:18583800-18595000 Weak transcription Fetal Stomach stomach
6 chr9:18584000-18603200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr9:18584200-18594800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
8 chr9:18584800-18595600 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
9 chr9:18587400-18588400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
10 chr9:18587400-18589200 Enhancers HSMM muscle
11 chr9:18587600-18588600 Enhancers NH-A brain
12 chr9:18587600-18588600 Enhancers NHDF-Ad bronchial
13 chr9:18587800-18588600 Enhancers Muscle Satellite Cultured Cells --
14 chr9:18588000-18588600 Enhancers HSMMtube muscle
15 chr9:18588200-18588600 Flanking Active TSS Osteobl bone
16 chr9:18588200-18588800 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow

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