Variant report
Variant | rs10444269 |
---|---|
Chromosome Location | chr11:33975771-33975772 |
allele | A/G |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr11:33974000-33976600 | Enhancers | Primary hematopoietic stem cells G-CSF-mobilized Female | -- |
2 | chr11:33974200-33975800 | Enhancers | Hela-S3 | cervix |
3 | chr11:33974600-33977400 | Weak transcription | Primary neutrophils fromperipheralblood | blood |
4 | chr11:33975000-33977000 | Enhancers | K562 | blood |
5 | chr11:33975000-33977200 | Enhancers | Primary hematopoietic stem cells G-CSF-mobilized Male | -- |
6 | chr11:33975200-33978400 | Weak transcription | Primary monocytes fromperipheralblood | blood |
7 | chr11:33975200-33978600 | Weak transcription | Fetal Adrenal Gland | Adrenal Gland |
8 | chr11:33975600-33977800 | Weak transcription | HUVEC | blood vessel |