Variant report
Variant | rs13051259 |
---|---|
Chromosome Location | chr21:39964867-39964868 |
allele | C/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr21:39955800-39971200 | Weak transcription | Primary hematopoietic stem cells G-CSF-mobilized Male | -- |
2 | chr21:39956600-39966000 | Weak transcription | Breast Myoepithelial Primary Cells | Breast |
3 | chr21:39964400-39965000 | Bivalent Enhancer | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |
4 | chr21:39964400-39968800 | Weak transcription | Spleen | Spleen |
5 | chr21:39964600-39965000 | Active TSS | Aorta | Aorta |
6 | chr21:39964600-39965200 | Bivalent/Poised TSS | NH-A | brain |
7 | chr21:39964800-39965200 | Flanking Bivalent TSS/Enh | Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells | embryonic stem cell |
8 | chr21:39964800-39965200 | Bivalent/Poised TSS | Osteobl | bone |