| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:58409212-58409656 | Common:14; Rare:153 | ||||
| chr19:58451334-58451734 | Common:9; Rare:253 | ||||
| chr19:58451813-58452213 | Common:12; Rare:117 | ||||
| chr19:58466785-58467185 | Common:6; Rare:459 | ||||
| chr19:58473226-58473540 | Common:5; Rare:79 | ||||
| chr19:58474088-58474498 | Rare:173 | ||||
| chr19:58475430-58476470 | Common:29; Rare:1224 | ||||
| chr19:58476391-58476497 | Rare:33 | ||||
| chr19:58476831-58476940 | Rare:35 | ||||
| chr19:58499150-58499687 | Common:21; Rare:1020; Clinvar:42; Clinvar (benign):12 | ||||
| chr19:58519075-58519197 | Rare:32 | ||||
| chr19:58519450-58519700 | Common:1; Rare:130 | ||||
| chr19:58519630-58520430 | Rare:687 | ||||
| chr19:58543827-58544227 | Common:5; Rare:387 | ||||
| chr19:58544132-58544557 | Common:20; Rare:814 |