| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:49813125-49813834 | Common:6; Rare:552 | ||||
| chr19:49817417-49817632 | Common:2; Rare:80 | ||||
| chr19:49818061-49818736 | Common:9; Rare:319; Clinvar:9; Clinvar (benign):5 | ||||
| chr19:49850026-49850426 | Rare:87 | ||||
| chr19:49850432-49850933 | Common:2; Rare:511 | ||||
| chr19:49850850-49851380 | Common:8; Rare:613 | ||||
| chr19:49851497-49851922 | Common:2; Rare:288 | ||||
| chr19:49856696-49857096 | Common:3; Rare:175; Clinvar (benign):1 | ||||
| chr19:49859851-49860481 | Common:5; Rare:330 | ||||
| chr19:49861541-49861941 | Common:3; Rare:301; Clinvar:22; Clinvar (benign):22; Clinvar (pathogenic):15 | ||||
| chr19:49865273-49865677 | Common:14; Rare:329; Clinvar:12; Clinvar (benign):10; Clinvar (pathogenic):2 | ||||
| chr19:49866277-49866677 | Common:3; Rare:222; Clinvar:2; Clinvar (benign):2 | ||||
| chr19:49866946-49867518 | Common:10; Rare:508; Clinvar:16; Clinvar (benign):43; Clinvar (pathogenic):3 | ||||
| chr19:49867451-49867966 | Common:18; Rare:422; Clinvar:5; Clinvar (benign):12 | ||||
| chr19:49875618-49876453 | Common:5; Rare:548 |