Variant report

Variant rs1644011
Chromosome Location chr12:44681578-44681579
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:44676600-44697800 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
2 chr12:44679200-44682000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
3 chr12:44679400-44681600 Enhancers HSMM muscle
4 chr12:44679600-44681800 Enhancers NHEK skin
5 chr12:44680200-44681600 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
6 chr12:44680200-44682000 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
7 chr12:44680400-44682000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr12:44680400-44682000 Enhancers HMEC breast
9 chr12:44680600-44681600 Enhancers Fetal Brain Female brain
10 chr12:44680600-44681800 Enhancers Osteobl bone
11 chr12:44680600-44682000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
12 chr12:44681000-44682000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
13 chr12:44681200-44681800 Weak transcription Fetal Brain Male brain
14 chr12:44681200-44684000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin

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