Variant report

Variant rs13392821
Chromosome Location chr2:20568500-20568501
allele A/C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:20551600-20568800 Weak transcription Psoas Muscle Psoas
2 chr2:20556800-20569200 Weak transcription Breast Myoepithelial Primary Cells Breast
3 chr2:20565000-20570200 Enhancers Placenta Placenta
4 chr2:20565200-20578400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
5 chr2:20565800-20569400 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
6 chr2:20565800-20570000 Weak transcription NHLF lung
7 chr2:20565800-20575200 Weak transcription NH-A brain
8 chr2:20567000-20571200 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
9 chr2:20567200-20568800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
10 chr2:20567200-20569000 Weak transcription NHEK skin
11 chr2:20567200-20569200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
12 chr2:20567200-20569200 Weak transcription HMEC breast
13 chr2:20567200-20569400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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