Variant report

Variant rs2471617
Chromosome Location chr12:46973129-46973130
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:46964000-46979400 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
2 chr12:46965200-46975200 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
3 chr12:46965200-46977600 Weak transcription Primary hematopoietic stem cells blood
4 chr12:46970000-46974600 Enhancers HepG2 liver
5 chr12:46971000-46973600 Enhancers Aorta Aorta
6 chr12:46971400-46973600 Weak transcription Primary B cells from cord blood blood
7 chr12:46972000-46973600 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
8 chr12:46972200-46979600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr12:46972400-46973200 Enhancers Psoas Muscle Psoas
10 chr12:46972400-46973800 Enhancers Stomach Smooth Muscle stomach
11 chr12:46972400-46984400 Weak transcription NHEK skin
12 chr12:46973000-46973400 Weak transcription Skeletal Muscle Male skeletal muscle

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