Variant report

Variant rs550747762
Chromosome Location chr20:14986322-14986323
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr20:14984600-14986400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
2 chr20:14984600-14986600 Enhancers Breast Myoepithelial Primary Cells Breast
3 chr20:14984600-14986800 Enhancers HMEC breast
4 chr20:14985000-14986600 Enhancers HepG2 liver
5 chr20:14985200-14986400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
6 chr20:14985200-14986600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr20:14985200-14986800 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
8 chr20:14985400-14986600 Enhancers NHEK skin
9 chr20:14985800-14986400 Enhancers Fetal Intestine Small intestine
10 chr20:14986000-14986400 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
11 chr20:14986000-14986400 Enhancers Fetal Intestine Large intestine
12 chr20:14986200-14986400 Enhancers H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
13 chr20:14986200-14986400 Enhancers Pancreas Pancrea
14 chr20:14986200-14986400 Enhancers A549 lung
15 chr20:14986200-14986600 Enhancers Fetal Heart heart
16 chr20:14986200-14986600 Enhancers Ovary ovary
17 chr20:14986200-14986600 Enhancers Stomach Mucosa stomach
18 chr20:14986200-14991000 Weak transcription Fetal Kidney kidney

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