Variant report

Variant rs190068824
Chromosome Location chr20:14986089-14986090
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr20:14983400-14986200 Weak transcription Pancreas Pancrea
2 chr20:14984600-14986200 Enhancers Fetal Kidney kidney
3 chr20:14984600-14986400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
4 chr20:14984600-14986600 Enhancers Breast Myoepithelial Primary Cells Breast
5 chr20:14984600-14986800 Enhancers HMEC breast
6 chr20:14984800-14986200 Enhancers HUES64 Cell Line embryonic stem cell
7 chr20:14985000-14986200 Weak transcription Ovary ovary
8 chr20:14985000-14986600 Enhancers HepG2 liver
9 chr20:14985200-14986400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
10 chr20:14985200-14986600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr20:14985200-14986800 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
12 chr20:14985400-14986600 Enhancers NHEK skin
13 chr20:14985800-14986200 Flanking Active TSS Stomach Mucosa stomach
14 chr20:14985800-14986400 Enhancers Fetal Intestine Small intestine
15 chr20:14986000-14986200 Flanking Active TSS Fetal Heart heart
16 chr20:14986000-14986400 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
17 chr20:14986000-14986400 Enhancers Fetal Intestine Large intestine

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