Variant report
Variant | rs73364007 |
---|---|
Chromosome Location | chr21:40734602-40734603 |
allele | A/G |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr21:40731000-40734800 | Weak transcription | Foreskin Keratinocyte Primary Cells skin02 | Skin |
2 | chr21:40731600-40734800 | Weak transcription | K562 | blood |
3 | chr21:40734000-40735000 | Enhancers | Primary monocytes fromperipheralblood | blood |
4 | chr21:40734000-40735000 | Enhancers | Monocytes-CD14+_RO01746 | blood |
5 | chr21:40734000-40736600 | Enhancers | Primary hematopoietic stem cells short term culture | blood |
6 | chr21:40734000-40736800 | Enhancers | Primary hematopoietic stem cells | blood |
7 | chr21:40734000-40737400 | Enhancers | Primary hematopoietic stem cells G-CSF-mobilized Female | -- |
8 | chr21:40734200-40734800 | Flanking Active TSS | Primary neutrophils fromperipheralblood | blood |
9 | chr21:40734400-40734800 | Flanking Active TSS | Primary hematopoietic stem cells G-CSF-mobilized Male | -- |
10 | chr21:40734400-40737800 | Enhancers | IMR90 fetal lung fibroblasts Cell Line | lung |
11 | chr21:40734600-40735000 | Bivalent Enhancer | Primary B cells from cord blood | blood |