Variant report

Variant rs17173164
Chromosome Location chr19:43685163-43685164
allele C/G/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:43683800-43685200 Weak transcription Placenta Placenta
2 chr19:43684000-43688400 Enhancers HMEC breast
3 chr19:43684200-43685200 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
4 chr19:43684200-43685200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr19:43684200-43685200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
6 chr19:43684200-43685200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
7 chr19:43684200-43685200 Weak transcription A549 lung
8 chr19:43684200-43685200 Weak transcription NHLF lung
9 chr19:43684200-43685200 Weak transcription Osteobl bone
10 chr19:43684600-43685200 Weak transcription Hela-S3 cervix
11 chr19:43684800-43685800 Enhancers NHEK skin
12 chr19:43685000-43685400 Genic enhancers NHDF-Ad bronchial
13 chr19:43685000-43686400 Enhancers Breast Myoepithelial Primary Cells Breast
14 chr19:43685000-43686600 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin

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