Variant report

Variant rs17783986
Chromosome Location chr7:64903762-64903763
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:64902400-64904800 Weak transcription HepG2 liver
2 chr7:64902800-64904000 Enhancers Osteobl bone
3 chr7:64902800-64904200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
4 chr7:64902800-64904800 Enhancers NHDF-Ad bronchial
5 chr7:64902800-64906600 Enhancers NHEK skin
6 chr7:64902800-64907200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
7 chr7:64902800-64907200 Enhancers HMEC breast
8 chr7:64903000-64904200 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
9 chr7:64903000-64904200 Enhancers NHLF lung
10 chr7:64903000-64906800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr7:64903200-64904200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
12 chr7:64903200-64904400 Enhancers HUVEC blood vessel
13 chr7:64903200-64907400 Enhancers NH-A brain
14 chr7:64903400-64904000 Enhancers Fetal Adrenal Gland Adrenal Gland
15 chr7:64903600-64904800 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell

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