Variant report
| Variant | rs60560949 |
|---|---|
| Chromosome Location | chr1:226989995-226989996 |
| allele | C/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr1:226985000-226990000 | Enhancers | Primary T cells from cord blood | blood |
| 2 | chr1:226987200-227001400 | Weak transcription | Right Atrium | heart |
| 3 | chr1:226987400-226991400 | Weak transcription | Lung | lung |
| 4 | chr1:226987400-226992000 | Weak transcription | Foreskin Melanocyte Primary Cells skin01 | Skin |
| 5 | chr1:226987400-226997400 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
| 6 | chr1:226988600-226990800 | Weak transcription | Thymus | Thymus |
| 7 | chr1:226988600-226992800 | Weak transcription | Primary T cells fromperipheralblood | blood |
| 8 | chr1:226988800-226990000 | Weak transcription | Fetal Thymus | thymus |
| 9 | chr1:226989400-227002800 | Weak transcription | Primary T helper naive cells fromperipheralblood | blood |
| 10 | chr1:226989600-226994200 | Weak transcription | Placenta Amnion | Placenta Amnion |
| 11 | chr1:226989800-226991400 | Weak transcription | K562 | blood |
