Variant report
Variant | rs2070526 |
---|---|
Chromosome Location | chr21:39971344-39971345 |
allele | C/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr21:39967000-39971400 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
2 | chr21:39969000-39976600 | Weak transcription | H9 Cell Line | embryonic stem cell |
3 | chr21:39969400-39973000 | Enhancers | Breast Myoepithelial Primary Cells | Breast |
4 | chr21:39970200-39977200 | Weak transcription | ES-UCSF4 Cell Line | embryonic stem cell |
5 | chr21:39970400-39972000 | Enhancers | Spleen | Spleen |
6 | chr21:39970400-39976600 | Weak transcription | Fetal Brain Male | brain |
7 | chr21:39971000-39971600 | Bivalent Enhancer | Fetal Muscle Trunk | muscle |
8 | chr21:39971200-39971800 | Enhancers | Adipose Nuclei | Adipose |
9 | chr21:39971200-39972000 | Enhancers | Primary hematopoietic stem cells G-CSF-mobilized Male | -- |
10 | chr21:39971200-39972400 | Bivalent Enhancer | Fetal Adrenal Gland | Adrenal Gland |