Variant report

Variant rs13238146
Chromosome Location chr7:98791364-98791365
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:98790600-98792200 Enhancers Fetal Adrenal Gland Adrenal Gland
2 chr7:98790800-98792200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
3 chr7:98790800-98792200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
4 chr7:98790800-98792200 Enhancers Stomach Mucosa stomach
5 chr7:98790800-98792200 Enhancers A549 lung
6 chr7:98790800-98792200 Enhancers Osteobl bone
7 chr7:98790800-98792400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr7:98790800-98792400 Enhancers HMEC breast
9 chr7:98790800-98792400 Enhancers NHEK skin
10 chr7:98791000-98792000 Enhancers Ovary ovary
11 chr7:98791000-98792200 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
12 chr7:98791000-98792200 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
13 chr7:98791000-98792200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
14 chr7:98791000-98792200 Enhancers NH-A brain
15 chr7:98791000-98792400 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
16 chr7:98791000-98792400 Enhancers NHDF-Ad bronchial
17 chr7:98791200-98792000 Enhancers Muscle Satellite Cultured Cells --
18 chr7:98791200-98792600 Weak transcription Spleen Spleen
19 chr7:98791200-98793400 Weak transcription HepG2 liver

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