Variant report

Variant rs17442924
Chromosome Location chr12:40552165-40552166
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:40547200-40558600 Weak transcription Liver Liver
2 chr12:40547800-40552200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
3 chr12:40548800-40553800 Weak transcription H1 Cell Line embryonic stem cell
4 chr12:40549600-40552200 Enhancers Primary monocytes fromperipheralblood blood
5 chr12:40550600-40552800 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
6 chr12:40550800-40553000 Enhancers Pancreatic Islets Pancreatic Islet
7 chr12:40551000-40553200 Flanking Active TSS Monocytes-CD14+_RO01746 blood
8 chr12:40551200-40552600 Enhancers HMEC breast
9 chr12:40551200-40553200 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
10 chr12:40551200-40553200 Enhancers Breast Myoepithelial Primary Cells Breast
11 chr12:40551200-40553200 Enhancers Muscle Satellite Cultured Cells --
12 chr12:40551200-40553600 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
13 chr12:40551600-40552200 Enhancers GM12878-XiMat blood
14 chr12:40551600-40553200 Enhancers Primary B cells from peripheral blood blood
15 chr12:40551800-40552200 Enhancers Primary neutrophils fromperipheralblood blood
16 chr12:40551800-40553200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
17 chr12:40551800-40553400 Enhancers NHEK skin
18 chr12:40552000-40552200 Weak transcription Primary hematopoietic stem cells blood
19 chr12:40552000-40553000 Flanking Active TSS Primary B cells from cord blood blood
20 chr12:40552000-40556200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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