| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:16572354-16572679 | Common:5; Rare:125 | ||||
| chr19:17215226-17215393 | Common:2; Rare:51 | ||||
| chr19:17405628-17405742 | Rare:19 | ||||
| chr19:17511575-17511673 | Common:1; Rare:51 | ||||
| chr19:18280859-18281062 | Rare:74 | ||||
| chr19:18919241-18919763 | Common:4; Rare:211 | ||||
| chr19:19033482-19033611 | Common:2; Rare:45 | ||||
| chr19:19192107-19192264 | Common:1; Rare:48 | ||||
| chr19:19192589-19193015 | Common:3; Rare:105; Clinvar (benign):1 | ||||
| chr19:19320480-19320857 | Common:4; Rare:137 | ||||
| chr19:19516160-19516250 | Rare:45 | ||||
| chr19:29213134-29213219 | Common:1; Rare:34 | ||||
| chr19:29606179-29606321 | Rare:48 | ||||
| chr19:31349225-31349518 | Common:4; Rare:98 | ||||
| chr19:32692250-32692390 | Common:2; Rare:77 |