| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:50384022-50384384 | Common:2; Rare:153; Clinvar:1; Clinvar (benign):2 | ||||
| chr19:50476209-50476542 | Common:1; Rare:156 | ||||
| chr19:50511211-50511401 | Common:1; Rare:58 | ||||
| chr19:50514634-50514806 | Common:2; Rare:45 | ||||
| chr19:50639795-50639951 | Common:3; Rare:50 | ||||
| chr19:50804587-50804897 | Common:5; Rare:93 | ||||
| chr19:51026588-51026814 | Common:2; Rare:56 | ||||
| chr19:51311578-51311901 | Common:4; Rare:65 | ||||
| chr19:51366333-51366551 | Common:5; Rare:58; Clinvar (benign):2 | ||||
| chr19:51751852-51751987 | Common:2; Rare:28 | ||||
| chr19:51887874-51888052 | Rare:63 | ||||
| chr19:51927146-51927482 | Common:1; Rare:94 | ||||
| chr19:52008130-52008359 | Rare:69 | ||||
| chr19:52028327-52028475 | Common:3; Rare:34 | ||||
| chr19:52048638-52048964 | Common:2; Rare:106 |