Variant report

Variant rs74129526
Chromosome Location chr1:173030666-173030667
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:173022400-173031000 Weak transcription HUVEC blood vessel
2 chr1:173025800-173030800 Weak transcription HMEC breast
3 chr1:173026000-173031400 Weak transcription Placenta Amnion Placenta Amnion
4 chr1:173028000-173030800 Weak transcription Fetal Lung lung
5 chr1:173030400-173032000 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
6 chr1:173030600-173030800 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
7 chr1:173030600-173032000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr1:173030600-173032200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
9 chr1:173030600-173032400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
10 chr1:173030600-173033200 Enhancers NHEK skin

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