Variant report
Variant | rs1375628 |
---|---|
Chromosome Location | chr14:81166689-81166690 |
allele | A/G |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr14:81147400-81171400 | Weak transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |
2 | chr14:81148000-81167400 | Weak transcription | Foreskin Keratinocyte Primary Cells skin02 | Skin |
3 | chr14:81148400-81167200 | Weak transcription | Fetal Thymus | thymus |
4 | chr14:81149000-81171200 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
5 | chr14:81160000-81168400 | Weak transcription | Primary T cells from cord blood | blood |
6 | chr14:81163200-81177800 | Weak transcription | A549 | lung |
7 | chr14:81165600-81169000 | Strong transcription | Dnd41 | blood |
8 | chr14:81165800-81168200 | Weak transcription | Esophagus | oesophagus |
9 | chr14:81166200-81168400 | Strong transcription | Thymus | Thymus |
10 | chr14:81166200-81180200 | Weak transcription | Primary hematopoietic stem cells short term culture | blood |
11 | chr14:81166400-81166800 | Enhancers | GM12878-XiMat | blood |