Variant report

Variant rs7778185
Chromosome Location chr7:64913759-64913760
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:64913200-64913800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
2 chr7:64913200-64914800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
3 chr7:64913200-64914800 Enhancers NH-A brain
4 chr7:64913200-64914800 Enhancers NHEK skin
5 chr7:64913200-64915000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr7:64913200-64915000 Enhancers HMEC breast
7 chr7:64913400-64914400 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
8 chr7:64913400-64914600 Enhancers Osteobl bone
9 chr7:64913400-64915000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
10 chr7:64913600-64914000 Enhancers Fetal Adrenal Gland Adrenal Gland
11 chr7:64913600-64914000 Weak transcription HepG2 liver
12 chr7:64913600-64914400 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
13 chr7:64913600-64914600 Enhancers NHDF-Ad bronchial
14 chr7:64913600-64915000 Enhancers HUVEC blood vessel

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