Variant report

Variant rs74129528
Chromosome Location chr1:173030870-173030871
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:173022400-173031000 Weak transcription HUVEC blood vessel
2 chr1:173026000-173031400 Weak transcription Placenta Amnion Placenta Amnion
3 chr1:173030400-173032000 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
4 chr1:173030600-173032000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr1:173030600-173032200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
6 chr1:173030600-173032400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
7 chr1:173030600-173033200 Enhancers NHEK skin
8 chr1:173030800-173031600 Enhancers Primary hematopoietic stem cells short term culture blood
9 chr1:173030800-173031600 Enhancers A549 lung
10 chr1:173030800-173031800 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
11 chr1:173030800-173032400 Enhancers HMEC breast
12 chr1:173030800-173033600 Enhancers Fetal Lung lung

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