Variant report

Variant rs7450140
Chromosome Location chr6:49293773-49293774
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:49288400-49293800 Weak transcription Primary hematopoietic stem cells blood
2 chr6:49293000-49293800 Enhancers NHEK skin
3 chr6:49293200-49295400 Enhancers HMEC breast
4 chr6:49293400-49293800 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
5 chr6:49293400-49293800 Enhancers Muscle Satellite Cultured Cells --
6 chr6:49293400-49294400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr6:49293400-49294600 Enhancers Osteobl bone
8 chr6:49293400-49295200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr6:49293400-49295200 Enhancers Hela-S3 cervix
10 chr6:49293600-49293800 Enhancers NHDF-Ad bronchial
11 chr6:49293600-49294000 Flanking Active TSS HUVEC blood vessel
12 chr6:49293600-49294600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
13 chr6:49293600-49295400 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
14 chr6:49293600-49295400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
15 chr6:49293600-49295800 Enhancers HSMM muscle
16 chr6:49293600-49296200 Enhancers Fetal Lung lung

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