Variant report
Variant | rs12088650 |
---|---|
Chromosome Location | chr1:174627698-174627699 |
allele | C/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr1:174607600-174628600 | Weak transcription | Primary T cells effector/memory enriched fromperipheralblood | blood |
2 | chr1:174607600-174637000 | Weak transcription | Primary B cells from peripheral blood | blood |
3 | chr1:174607600-174677800 | Weak transcription | Primary B cells from cord blood | blood |
4 | chr1:174612400-174638200 | Weak transcription | Aorta | Aorta |
5 | chr1:174613600-174637000 | Weak transcription | Primary T cells from cord blood | blood |
6 | chr1:174623200-174628600 | Weak transcription | Fetal Heart | heart |
7 | chr1:174625400-174636600 | Weak transcription | Primary T cells fromperipheralblood | blood |
8 | chr1:174625800-174634800 | Weak transcription | GM12878-XiMat | blood |
9 | chr1:174626000-174628400 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
10 | chr1:174626200-174629400 | Weak transcription | Fetal Brain Male | brain |
11 | chr1:174626400-174628600 | Weak transcription | HepG2 | liver |
12 | chr1:174627600-174630800 | Weak transcription | Primary T helper 17 cells PMA-I stimulated | -- |