Variant report

Variant rs34350957
Chromosome Location chr7:98791011-98791012
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:98790600-98791200 Enhancers HepG2 liver
2 chr7:98790600-98792200 Enhancers Fetal Adrenal Gland Adrenal Gland
3 chr7:98790800-98792200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
4 chr7:98790800-98792200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
5 chr7:98790800-98792200 Enhancers Stomach Mucosa stomach
6 chr7:98790800-98792200 Enhancers A549 lung
7 chr7:98790800-98792200 Enhancers Osteobl bone
8 chr7:98790800-98792400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr7:98790800-98792400 Enhancers HMEC breast
10 chr7:98790800-98792400 Enhancers NHEK skin
11 chr7:98791000-98791200 Enhancers Spleen Spleen
12 chr7:98791000-98792000 Enhancers Ovary ovary
13 chr7:98791000-98792200 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
14 chr7:98791000-98792200 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
15 chr7:98791000-98792200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
16 chr7:98791000-98792200 Enhancers NH-A brain
17 chr7:98791000-98792400 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
18 chr7:98791000-98792400 Enhancers NHDF-Ad bronchial

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