Variant report

Variant rs11048409
Chromosome Location chr12:26250878-26250879
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:26244600-26254200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
2 chr12:26245200-26254000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
3 chr12:26249800-26251000 Enhancers NHEK skin
4 chr12:26250200-26251000 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
5 chr12:26250200-26251000 Enhancers Muscle Satellite Cultured Cells --
6 chr12:26250200-26252400 Weak transcription Fetal Intestine Large intestine
7 chr12:26250400-26251000 Enhancers NHDF-Ad bronchial
8 chr12:26250400-26253000 Weak transcription Fetal Intestine Small intestine
9 chr12:26250600-26251000 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
10 chr12:26250600-26251000 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
11 chr12:26250600-26251000 Enhancers HSMM muscle
12 chr12:26250600-26251400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
13 chr12:26250600-26254000 Weak transcription Stomach Mucosa stomach
14 chr12:26250600-26254200 Weak transcription Breast Myoepithelial Primary Cells Breast
15 chr12:26250800-26254000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
16 chr12:26250800-26254000 Weak transcription HMEC breast

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