Variant report

Variant rs11831929
Chromosome Location chr12:46965257-46965258
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:46961600-46970800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr12:46963000-46971200 Weak transcription Primary B cells from cord blood blood
3 chr12:46963200-46966400 Weak transcription Hela-S3 cervix
4 chr12:46963400-46965600 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
5 chr12:46963800-46970800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr12:46963800-46971000 Weak transcription Aorta Aorta
7 chr12:46964000-46979400 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
8 chr12:46964800-46965800 Enhancers NHDF-Ad bronchial
9 chr12:46964800-46969400 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
10 chr12:46965000-46967800 Enhancers HSMMtube muscle
11 chr12:46965200-46975200 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
12 chr12:46965200-46977600 Weak transcription Primary hematopoietic stem cells blood

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