Variant report
Variant | rs9668289 |
---|---|
Chromosome Location | chr12:62522051-62522052 |
allele | A/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr12:62519800-62525600 | Weak transcription | Pancreatic Islets | Pancreatic Islet |
2 | chr12:62521400-62522400 | Enhancers | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
3 | chr12:62521400-62522600 | Enhancers | Foreskin Keratinocyte Primary Cells skin02 | Skin |
4 | chr12:62521400-62522600 | Enhancers | Foreskin Keratinocyte Primary Cells skin03 | Skin |
5 | chr12:62521400-62522600 | Enhancers | HMEC | breast |
6 | chr12:62521600-62522200 | Enhancers | Primary hematopoietic stem cells G-CSF-mobilized Female | -- |
7 | chr12:62521600-62522200 | Enhancers | Primary hematopoietic stem cells G-CSF-mobilized Male | -- |
8 | chr12:62521600-62522600 | Enhancers | Fetal Adrenal Gland | Adrenal Gland |
9 | chr12:62521800-62522400 | Enhancers | NHEK | skin |
10 | chr12:62522000-62523000 | Enhancers | Primary hematopoietic stem cells | blood |
11 | chr12:62522000-62523000 | Bivalent Enhancer | HUVEC | blood vessel |