| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:16324543-16324836 | Common:2; Rare:82 | ||||
| chr19:16471938-16472192 | Common:5; Rare:79 | ||||
| chr19:16542376-16542605 | Common:2; Rare:70 | ||||
| chr19:16572348-16572615 | Common:5; Rare:114 | ||||
| chr19:17215266-17215402 | Common:2; Rare:49 | ||||
| chr19:17226133-17226250 | Common:2; Rare:43 | ||||
| chr19:17305687-17305889 | Common:1; Rare:85 | ||||
| chr19:17337543-17337559 | Rare:4 | ||||
| chr19:17405574-17405656 | Common:1; Rare:19 | ||||
| chr19:17405659-17405822 | Common:4; Rare:19 | ||||
| chr19:17511612-17511670 | Rare:24 | ||||
| chr19:17512132-17512355 | Rare:67 | ||||
| chr19:17523243-17523455 | Common:1; Rare:62 | ||||
| chr19:17751369-17751537 | Common:1; Rare:40 | ||||
| chr19:17847941-17848169 | Common:1; Rare:50; Clinvar:1; Clinvar (benign):1 |