Variant report
Variant | rs6718158 |
---|---|
Chromosome Location | chr2:145430636-145430637 |
allele | A/G |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:145416800-145431400 | Enhancers | Primary monocytes fromperipheralblood | blood |
2 | chr2:145419000-145432800 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
3 | chr2:145423000-145440600 | Weak transcription | Primary hematopoietic stem cells | blood |
4 | chr2:145424000-145433000 | Weak transcription | HMEC | breast |
5 | chr2:145429400-145430800 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |
6 | chr2:145429800-145432200 | Weak transcription | Primary hematopoietic stem cells short term culture | blood |
7 | chr2:145430600-145431400 | Enhancers | Fetal Kidney | kidney |
8 | chr2:145430600-145431400 | Enhancers | Monocytes-CD14+_RO01746 | blood |