Variant report

Variant rs17091108
Chromosome Location chr1:71777555-71777556
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:71770600-71781200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr1:71773600-71778000 Weak transcription HUVEC blood vessel
3 chr1:71776800-71778200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
4 chr1:71777000-71778000 Enhancers NHDF-Ad bronchial
5 chr1:71777000-71778200 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
6 chr1:71777200-71777600 Enhancers Breast Myoepithelial Primary Cells Breast
7 chr1:71777200-71777600 Enhancers Muscle Satellite Cultured Cells --
8 chr1:71777200-71778000 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
9 chr1:71777200-71778400 Enhancers Liver Liver
10 chr1:71777200-71778800 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin

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