Variant report

Variant rs16874332
Chromosome Location chr8:107312721-107312722
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:107284800-107331800 Weak transcription Aorta Aorta
2 chr8:107302200-107322600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
3 chr8:107308600-107333400 Weak transcription Cortex derived primary cultured neurospheres brain
4 chr8:107308600-107348600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr8:107312000-107313200 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
6 chr8:107312000-107313200 Enhancers NHDF-Ad bronchial
7 chr8:107312000-107313400 Enhancers Muscle Satellite Cultured Cells --
8 chr8:107312000-107313400 Enhancers HUVEC blood vessel
9 chr8:107312200-107313200 Enhancers Osteobl bone
10 chr8:107312400-107313000 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
11 chr8:107312400-107313000 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
12 chr8:107312400-107313200 Enhancers NH-A brain
13 chr8:107312400-107313400 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
14 chr8:107312600-107313000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived

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