Variant report

Variant rs970249
Chromosome Location chr12:58421132-58421133
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:58419200-58422200 Enhancers Stomach Smooth Muscle stomach
2 chr12:58419200-58423400 Weak transcription Esophagus oesophagus
3 chr12:58419800-58421800 Enhancers Fetal Muscle Leg muscle
4 chr12:58420200-58422400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
5 chr12:58420400-58421200 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
6 chr12:58420400-58421200 Enhancers Cortex derived primary cultured neurospheres brain
7 chr12:58420400-58421400 Enhancers Fetal Kidney kidney
8 chr12:58420400-58421600 Enhancers Adipose Nuclei Adipose
9 chr12:58421000-58421200 Enhancers Brain Hippocampus Middle brain
10 chr12:58421000-58421400 Enhancers HMEC breast
11 chr12:58421000-58422000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
12 chr12:58421000-58422000 Weak transcription NHEK skin
13 chr12:58421000-58425600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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