Variant report

Variant rs10100830
Chromosome Location chr8:129893934-129893935
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:129881600-129894200 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
2 chr8:129887200-129894000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
3 chr8:129887400-129894800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr8:129887400-129896000 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
5 chr8:129890400-129895800 Weak transcription NHLF lung
6 chr8:129890600-129894200 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
7 chr8:129890800-129894200 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
8 chr8:129893000-129897000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
9 chr8:129893000-129897000 Enhancers NHDF-Ad bronchial
10 chr8:129893600-129896600 Enhancers Muscle Satellite Cultured Cells --
11 chr8:129893800-129896400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
12 chr8:129893800-129896800 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin

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