Variant report
| Variant | rs6728757 |
|---|---|
| Chromosome Location | chr2:55139656-55139657 |
| allele | A/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr2:55095200-55148200 | Weak transcription | Primary B cells from peripheral blood | blood |
| 2 | chr2:55132000-55140600 | Weak transcription | Esophagus | oesophagus |
| 3 | chr2:55134000-55153800 | Weak transcription | Brain Angular Gyrus | brain |
| 4 | chr2:55134200-55147600 | Weak transcription | Fetal Brain Female | brain |
| 5 | chr2:55134400-55153600 | Weak transcription | Brain Inferior Temporal Lobe | brain |
| 6 | chr2:55136200-55140400 | Weak transcription | IMR90 fetal lung fibroblasts Cell Line | lung |
| 7 | chr2:55136200-55145600 | Weak transcription | HepG2 | liver |
| 8 | chr2:55136800-55140400 | Weak transcription | Foreskin Fibroblast Primary Cells skin01 | Skin |
| 9 | chr2:55136800-55142000 | Weak transcription | Foreskin Fibroblast Primary Cells skin02 | Skin |
| 10 | chr2:55137800-55140400 | Weak transcription | NHDF-Ad | bronchial |
| 11 | chr2:55139600-55139800 | Enhancers | NHLF | lung |
| 12 | chr2:55139600-55140200 | Weak transcription | K562 | blood |
