| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:6416754-6417007 | Common:1; Rare:84 | ||||
| chr19:6480524-6480535 | Rare:1 | ||||
| chr19:6481725-6481821 | Common:1; Rare:27 | ||||
| chr19:6772602-6772745 | Rare:29 | ||||
| chr19:7069674-7069737 | Common:1; Rare:16 | ||||
| chr19:7394900-7395163 | Common:5; Rare:69 | ||||
| chr19:7492193-7492499 | Rare:66 | ||||
| chr19:7533826-7534202 | Common:3; Rare:102; Clinvar (benign):1 | ||||
| chr19:7535326-7535778 | Common:4; Rare:136; Clinvar:2 | ||||
| chr19:7629535-7629887 | Common:5; Rare:123; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr19:7636978-7637181 | Common:2; Rare:61; Clinvar (benign):1 | ||||
| chr19:7645823-7645997 | Common:2; Rare:32 | ||||
| chr19:7676932-7677174 | Common:2; Rare:60 | ||||
| chr19:7920179-7920393 | Rare:83 | ||||
| chr19:8321322-8321653 | Common:2; Rare:145 |