Variant report

Variant rs12036771
Chromosome Location chr1:221844882-221844883
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:221841600-221848400 Weak transcription Stomach Mucosa stomach
2 chr1:221842200-221846000 Enhancers HMEC breast
3 chr1:221842600-221845800 Enhancers NHDF-Ad bronchial
4 chr1:221842600-221846200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
5 chr1:221842600-221846800 Enhancers HSMM muscle
6 chr1:221843000-221845600 Enhancers Osteobl bone
7 chr1:221843000-221846000 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
8 chr1:221843000-221846400 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
9 chr1:221843000-221846800 Enhancers Muscle Satellite Cultured Cells --
10 chr1:221843000-221847600 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
11 chr1:221843600-221847800 Weak transcription Breast Myoepithelial Primary Cells Breast
12 chr1:221844000-221845400 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
13 chr1:221844600-221845000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
14 chr1:221844800-221845800 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
15 chr1:221844800-221846000 Enhancers Fetal Adrenal Gland Adrenal Gland

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