Variant report

Variant rs534026921
Chromosome Location chr7:110182949-110182950
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:110175200-110188400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr7:110180400-110183200 Enhancers HMEC breast
3 chr7:110181000-110184600 Enhancers NHEK skin
4 chr7:110181400-110183200 Enhancers NHLF lung
5 chr7:110182600-110183200 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
6 chr7:110182600-110184200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr7:110182600-110185200 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
8 chr7:110182800-110183000 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
9 chr7:110182800-110183800 Weak transcription NH-A brain

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