Variant report

Variant rs71371441
Chromosome Location chr17:38853457-38853458
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr17:38850000-38854000 Enhancers Placenta Placenta
2 chr17:38851000-38854000 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
3 chr17:38852000-38854600 Enhancers Fetal Kidney kidney
4 chr17:38852200-38854000 Enhancers Breast Myoepithelial Primary Cells Breast
5 chr17:38852200-38854000 Enhancers Fetal Lung lung
6 chr17:38852600-38853800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr17:38852600-38853800 Enhancers NHEK skin
8 chr17:38852600-38854000 Enhancers Hela-S3 cervix
9 chr17:38852800-38853600 Bivalent Enhancer HepG2 liver
10 chr17:38852800-38853800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr17:38852800-38854000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
12 chr17:38852800-38854000 Enhancers HMEC breast
13 chr17:38853000-38859800 Weak transcription Pancreas Pancrea
14 chr17:38853200-38853800 Weak transcription Fetal Intestine Large intestine
15 chr17:38853200-38854200 Weak transcription Pancreatic Islets Pancreatic Islet
16 chr17:38853200-38856200 Weak transcription Gastric stomach
17 chr17:38853200-38858400 Enhancers Placenta Amnion Placenta Amnion
18 chr17:38853400-38853800 Enhancers Liver Liver
19 chr17:38853400-38855400 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
20 chr17:38853400-38864000 Weak transcription A549 lung

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