Variant report

Variant rs79181287
Chromosome Location chr20:52392185-52392186
allele -/A/AA
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr20:52381000-52394600 Weak transcription Right Atrium heart
2 chr20:52384400-52394800 Weak transcription Duodenum Mucosa Duodenum
3 chr20:52385400-52392400 Weak transcription H9 Cell Line embryonic stem cell
4 chr20:52389400-52392200 Enhancers Breast Myoepithelial Primary Cells Breast
5 chr20:52390200-52403400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
6 chr20:52390400-52395000 Enhancers HepG2 liver
7 chr20:52390600-52394200 Weak transcription Liver Liver
8 chr20:52391200-52394400 Weak transcription Skeletal Muscle Male skeletal muscle
9 chr20:52391400-52392400 Enhancers HSMM muscle
10 chr20:52391400-52394600 Weak transcription Placenta Placenta
11 chr20:52391400-52394600 Weak transcription Stomach Mucosa stomach
12 chr20:52391600-52392400 Enhancers NHDF-Ad bronchial
13 chr20:52391600-52394600 Weak transcription Small Intestine intestine
14 chr20:52391800-52393200 Enhancers A549 lung
15 chr20:52391800-52394400 Weak transcription Pancreas Pancrea
16 chr20:52391800-52394800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
17 chr20:52392000-52394400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
18 chr20:52392000-52394400 Weak transcription NHEK skin
19 chr20:52392000-52394800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
20 chr20:52392000-52394800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
21 chr20:52392000-52394800 Weak transcription HMEC breast

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