Variant report

Variant rs73385409
Chromosome Location chr8:129896657-129896658
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:129893000-129897000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
2 chr8:129893000-129897000 Enhancers NHDF-Ad bronchial
3 chr8:129893800-129896800 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
4 chr8:129894000-129896800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
5 chr8:129894200-129897000 Enhancers NHEK skin
6 chr8:129894400-129897000 Enhancers HMEC breast
7 chr8:129894800-129896800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr8:129895800-129897000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr8:129896400-129901200 Weak transcription NHLF lung
10 chr8:129896400-129902400 Weak transcription HSMM muscle
11 chr8:129896400-129902800 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
12 chr8:129896400-129902800 Weak transcription Osteobl bone

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