Variant report

Variant rs117850132
Chromosome Location chr11:16531336-16531337
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:6 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:16510400-16533000 Weak transcription Fetal Heart heart
2 chr11:16528000-16531400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
3 chr11:16528000-16533400 Weak transcription Cortex derived primary cultured neurospheres brain
4 chr11:16530800-16531800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr11:16530800-16531800 Enhancers NHEK skin
6 chr11:16531200-16531600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin

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