Variant report
| Variant | rs61809308 |
|---|---|
| Chromosome Location | chr1:180629823-180629824 |
| allele | C/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr1:180602000-180645200 | Weak transcription | Gastric | stomach |
| 2 | chr1:180613200-180632600 | Weak transcription | Aorta | Aorta |
| 3 | chr1:180619600-180632600 | Weak transcription | Pancreas | Pancrea |
| 4 | chr1:180619600-180634600 | Weak transcription | ES-UCSF4 Cell Line | embryonic stem cell |
| 5 | chr1:180625800-180634800 | Weak transcription | H1 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
| 6 | chr1:180627600-180632800 | Weak transcription | A549 | lung |
| 7 | chr1:180627600-180640000 | Weak transcription | Fetal Heart | heart |
| 8 | chr1:180627800-180634200 | Weak transcription | hESC Derived CD56+ Ectoderm Cultured Cells | ES cell derived |
| 9 | chr1:180628200-180631600 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
| 10 | chr1:180629200-180633800 | Weak transcription | Sigmoid Colon | Sigmoid Colon |
| 11 | chr1:180629600-180632600 | Weak transcription | Primary T helper cells fromperipheralblood | blood |
| 12 | chr1:180629600-180641000 | Weak transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |
