Variant report

Variant rs55898202
Chromosome Location chr3:150504405-150504406
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:150500200-150505400 Weak transcription Brain Substantia Nigra brain
2 chr3:150501800-150506000 Enhancers NHEK skin
3 chr3:150502800-150504600 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
4 chr3:150502800-150504600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr3:150502800-150505600 Weak transcription Primary T helper cells PMA-I stimulated --
6 chr3:150503000-150505400 Weak transcription Primary T helper 17 cells PMA-I stimulated --
7 chr3:150503200-150504800 Weak transcription GM12878-XiMat blood
8 chr3:150503200-150505800 Enhancers Placenta Placenta
9 chr3:150503200-150505800 Weak transcription Osteobl bone
10 chr3:150504000-150504800 Enhancers Placenta Amnion Placenta Amnion
11 chr3:150504000-150505600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
12 chr3:150504000-150506000 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
13 chr3:150504200-150505800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin

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