Variant report

Variant rs555044922
Chromosome Location chr11:104963426-104963427
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:104962600-104963600 Enhancers Primary monocytes fromperipheralblood blood
2 chr11:104962800-104963600 Enhancers Monocytes-CD14+_RO01746 blood
3 chr11:104962800-104964000 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
4 chr11:104962800-104964400 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
5 chr11:104963000-104964400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr11:104963200-104964000 Enhancers Hela-S3 cervix
7 chr11:104963200-104964200 Flanking Active TSS NHEK skin
8 chr11:104963400-104963600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr11:104963400-104963800 Active TSS Breast Myoepithelial Primary Cells Breast
10 chr11:104963400-104963800 Flanking Active TSS Foreskin Keratinocyte Primary Cells skin02 Skin
11 chr11:104963400-104963800 Flanking Active TSS HMEC breast
12 chr11:104963400-104970200 Weak transcription Primary hematopoietic stem cells short term culture blood

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