Variant report
| Variant | rs7965013 |
|---|---|
| Chromosome Location | chr12:121084837-121084838 |
| allele | A/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr12:121079600-121086800 | Weak transcription | Right Atrium | heart |
| 2 | chr12:121083800-121085200 | Enhancers | Brain Inferior Temporal Lobe | brain |
| 3 | chr12:121084600-121085000 | Flanking Active TSS | Brain Anterior Caudate | brain |
| 4 | chr12:121084600-121085000 | Enhancers | Brain Cingulate Gyrus | brain |
| 5 | chr12:121084600-121085000 | Bivalent Enhancer | Skeletal Muscle Female | skeletal muscle |
| 6 | chr12:121084600-121085200 | Enhancers | Primary B cells from peripheral blood | blood |
| 7 | chr12:121084600-121085200 | Bivalent Enhancer | Primary T helper cells PMA-I stimulated | -- |
| 8 | chr12:121084600-121085200 | Enhancers | Primary T helper 17 cells PMA-I stimulated | -- |
| 9 | chr12:121084600-121085400 | Enhancers | Brain Angular Gyrus | brain |
| 10 | chr12:121084600-121085400 | Enhancers | Brain Dorsolateral Prefrontal Cortex | brain |
| 11 | chr12:121084800-121085000 | Bivalent Enhancer | Primary T cells fromperipheralblood | blood |
| 12 | chr12:121084800-121085000 | Enhancers | Brain Substantia Nigra | brain |
| 13 | chr12:121084800-121085000 | Enhancers | Esophagus | oesophagus |
| 14 | chr12:121084800-121085000 | Bivalent Enhancer | HepG2 | liver |
| 15 | chr12:121084800-121085000 | Bivalent Enhancer | NH-A | brain |
| 16 | chr12:121084800-121085200 | Enhancers | Primary B cells from cord blood | blood |
| 17 | chr12:121084800-121085200 | Bivalent Enhancer | Primary T killer naive cells fromperipheralblood | blood |
| 18 | chr12:121084800-121085400 | Enhancers | GM12878-XiMat | blood |
| 19 | chr12:121084800-121086600 | Weak transcription | Foreskin Fibroblast Primary Cells skin02 | Skin |
| 20 | chr12:121084800-121086600 | Weak transcription | Skeletal Muscle Male | skeletal muscle |
