Variant report

Variant rs150297572
Chromosome Location chr10:5091174-5091175
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:5088800-5091400 Enhancers Duodenum Mucosa Duodenum
2 chr10:5089200-5091600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
3 chr10:5089400-5091600 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
4 chr10:5089800-5091200 Enhancers Liver Liver
5 chr10:5089800-5091800 Enhancers HepG2 liver
6 chr10:5090000-5091200 Enhancers Muscle Satellite Cultured Cells --
7 chr10:5090000-5091200 Enhancers NHEK skin
8 chr10:5090000-5091200 Enhancers Osteobl bone
9 chr10:5090200-5091200 Enhancers HMEC breast
10 chr10:5090200-5091200 Enhancers HSMM muscle
11 chr10:5090600-5092600 Enhancers A549 lung
12 chr10:5090800-5091200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
13 chr10:5090800-5091200 Flanking Active TSS NHDF-Ad bronchial
14 chr10:5091000-5091200 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
15 chr10:5091000-5091200 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
16 chr10:5091000-5091200 Enhancers Sigmoid Colon Sigmoid Colon
17 chr10:5091000-5091200 Enhancers NHLF lung
18 chr10:5091000-5091400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
19 chr10:5091000-5097000 Weak transcription Stomach Mucosa stomach

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