Variant report

Variant rs1675756
Chromosome Location chr12:44279540-44279541
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:44240400-44293000 Weak transcription Aorta Aorta
2 chr12:44256400-44285600 Weak transcription HSMMtube muscle
3 chr12:44274600-44286000 Weak transcription Pancreas Pancrea
4 chr12:44275000-44281200 Weak transcription Skeletal Muscle Male skeletal muscle
5 chr12:44277000-44279600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr12:44277800-44279600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
7 chr12:44278400-44279800 Enhancers Brain Angular Gyrus brain
8 chr12:44278400-44280200 Enhancers Breast Myoepithelial Primary Cells Breast
9 chr12:44278600-44279800 Enhancers Brain Cingulate Gyrus brain
10 chr12:44278600-44285800 Weak transcription Osteobl bone
11 chr12:44278600-44287400 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
12 chr12:44279000-44280200 Enhancers Pancreatic Islets Pancreatic Islet
13 chr12:44279200-44279800 Enhancers HMEC breast
14 chr12:44279200-44286200 Weak transcription Stomach Smooth Muscle stomach
15 chr12:44279200-44292600 Weak transcription Left Ventricle heart
16 chr12:44279200-44297600 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin

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