Variant report

Variant rs539839078
Chromosome Location chr11:104963310-104963311
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 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 chr11:104963000-104963400 Weak transcription Breast Myoepithelial Primary Cells Breast
6 chr11:104963000-104963400 Enhancers Primary hematopoietic stem cells short term culture blood
7 chr11:104963000-104963400 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
8 chr11:104963000-104964400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr11:104963200-104963400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
10 chr11:104963200-104963400 Flanking Active TSS Foreskin Keratinocyte Primary Cells skin03 Skin
11 chr11:104963200-104963400 Active TSS HMEC breast
12 chr11:104963200-104964000 Enhancers Hela-S3 cervix
13 chr11:104963200-104964200 Flanking Active TSS NHEK skin

Quick Search:


  
Input of quick search could be:

what's new

Quick links