Variant report

Variant rs11600402
Chromosome Location chr11:34691751-34691752
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:34688800-34692000 Enhancers Pancreatic Islets Pancreatic Islet
2 chr11:34689800-34702000 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
3 chr11:34690000-34702200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
4 chr11:34690200-34693400 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
5 chr11:34690200-34702000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr11:34691200-34691800 Enhancers Primary monocytes fromperipheralblood blood
7 chr11:34691200-34691800 Enhancers Primary hematopoietic stem cells short term culture blood
8 chr11:34691200-34692000 Enhancers Primary B cells from peripheral blood blood
9 chr11:34691200-34700600 Weak transcription A549 lung
10 chr11:34691400-34691800 Enhancers Primary T helper memory cells from peripheral blood 1 blood
11 chr11:34691400-34692000 Enhancers Primary T killer memory cells from peripheral blood blood
12 chr11:34691600-34692200 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
13 chr11:34691600-34693000 Weak transcription HepG2 liver

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