Variant report
Variant | rs10241929 |
---|---|
Chromosome Location | chr7:18711303-18711304 |
allele | A/C |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr7:18645400-18721000 | Weak transcription | Psoas Muscle | Psoas |
2 | chr7:18678400-18721200 | Weak transcription | Brain Substantia Nigra | brain |
3 | chr7:18688400-18715200 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |
4 | chr7:18688800-18746400 | Weak transcription | Primary hematopoietic stem cells | blood |
5 | chr7:18689400-18713200 | Weak transcription | Ganglion Eminence derived primary cultured neurospheres | brain |
6 | chr7:18696200-18715000 | Weak transcription | Primary Natural Killer cells fromperipheralblood | blood |
7 | chr7:18698000-18743400 | Weak transcription | HSMMtube | muscle |
8 | chr7:18699600-18776000 | Weak transcription | Aorta | Aorta |
9 | chr7:18703600-18713800 | Weak transcription | Primary hematopoietic stem cells G-CSF-mobilized Male | -- |
10 | chr7:18709200-18711600 | Strong transcription | Primary monocytes fromperipheralblood | blood |
11 | chr7:18709800-18715800 | Strong transcription | Primary B cells from cord blood | blood |
12 | chr7:18710600-18711400 | Enhancers | NHEK | skin |
13 | chr7:18710600-18711600 | Enhancers | HMEC | breast |
14 | chr7:18710800-18711600 | Enhancers | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
15 | chr7:18711000-18711600 | Strong transcription | Primary B cells from peripheral blood | blood |
16 | chr7:18711200-18711400 | Strong transcription | Monocytes-CD14+_RO01746 | blood |