Variant report

Variant rs574138516
Chromosome Location chr3:100300711-100300712
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:100276800-100309200 Weak transcription NH-A brain
2 chr3:100277600-100304200 Weak transcription Ovary ovary
3 chr3:100278200-100305800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
4 chr3:100289600-100301000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
5 chr3:100297600-100303400 Weak transcription Fetal Stomach stomach
6 chr3:100298600-100309000 Weak transcription Pancreas Pancrea
7 chr3:100298800-100301800 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
8 chr3:100298800-100301800 Weak transcription Placenta Amnion Placenta Amnion
9 chr3:100300000-100301800 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
10 chr3:100300200-100300800 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
11 chr3:100300200-100301600 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
12 chr3:100300200-100301600 Enhancers Osteobl bone
13 chr3:100300400-100300800 Enhancers Duodenum Mucosa Duodenum
14 chr3:100300400-100301000 Enhancers Muscle Satellite Cultured Cells --
15 chr3:100300400-100301600 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
16 chr3:100300600-100300800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
17 chr3:100300600-100309200 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin

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