The 2.0 version of rSNPBase

Variant report

Variant rs11046308
Chromosome Location chr12:22256278-22256279
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:22253600-22256800 Enhancers Primary hematopoietic stem cells short term culture blood
2 chr12:22253800-22256400 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
3 chr12:22254000-22256600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
4 chr12:22254200-22256400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
5 chr12:22254800-22256600 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
6 chr12:22255400-22258400 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
7 chr12:22255400-22262200 Weak transcription Primary T helper memory cells from peripheral blood 1 blood
8 chr12:22255600-22256800 Weak transcription Right Ventricle heart
9 chr12:22255600-22257800 Weak transcription HSMM muscle
10 chr12:22255600-22258200 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
11 chr12:22255800-22257800 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
12 chr12:22255800-22258000 Weak transcription NHDF-Ad bronchial
13 chr12:22256000-22258200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
14 chr12:22256000-22271000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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Last update: Aug 31, 2015