Variant report

Variant rs11960559
Chromosome Location chr5:112782829-112782830
allele A/C/G
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:112762000-112786000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr5:112764600-112786400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
3 chr5:112764800-112786800 Weak transcription NHEK skin
4 chr5:112770400-112783400 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
5 chr5:112770600-112786800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr5:112780400-112787400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr5:112781600-112784000 Enhancers Fetal Heart heart
8 chr5:112782200-112789600 Enhancers Fetal Stomach stomach
9 chr5:112782600-112783600 Weak transcription Fetal Lung lung

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