Variant report

Variant rs1519851
Chromosome Location chr8:129895819-129895820
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:129887400-129896000 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
2 chr8:129893000-129897000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
3 chr8:129893000-129897000 Enhancers NHDF-Ad bronchial
4 chr8:129893600-129896600 Enhancers Muscle Satellite Cultured Cells --
5 chr8:129893800-129896400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
6 chr8:129893800-129896800 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
7 chr8:129894000-129896800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
8 chr8:129894200-129896400 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
9 chr8:129894200-129896400 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
10 chr8:129894200-129897000 Enhancers NHEK skin
11 chr8:129894400-129897000 Enhancers HMEC breast
12 chr8:129894800-129896800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
13 chr8:129895200-129896400 Enhancers Placenta Placenta
14 chr8:129895800-129896200 Enhancers NH-A brain
15 chr8:129895800-129896400 Enhancers HSMM muscle
16 chr8:129895800-129896400 Enhancers NHLF lung
17 chr8:129895800-129897000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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