Variant report

Variant rs2471618
Chromosome Location chr12:46972145-46972146
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 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 chr12:46965800-46972200 Weak transcription NHDF-Ad bronchial
5 chr12:46967600-46972600 Weak transcription Primary B cells from peripheral blood blood
6 chr12:46967800-46972400 Weak transcription Psoas Muscle Psoas
7 chr12:46967800-46972400 Weak transcription Skeletal Muscle Male skeletal muscle
8 chr12:46968000-46972400 Weak transcription Skeletal Muscle Female skeletal muscle
9 chr12:46970000-46974600 Enhancers HepG2 liver
10 chr12:46970800-46972200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr12:46970800-46972200 Enhancers HMEC breast
12 chr12:46971000-46972200 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
13 chr12:46971000-46973600 Enhancers Aorta Aorta
14 chr12:46971400-46973600 Weak transcription Primary B cells from cord blood blood
15 chr12:46971600-46972400 Enhancers NHEK skin
16 chr12:46972000-46972600 Enhancers HSMMtube muscle
17 chr12:46972000-46973600 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell

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