| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:12611388-12611551 | Common:2; Rare:34 | ||||
| chr19:12666662-12666866 | Rare:204; Clinvar:12 | ||||
| chr19:12668337-12669297 | Common:4; Rare:343 | ||||
| chr19:12681198-12681622 | Common:6; Rare:376 | ||||
| chr19:12681607-12682106 | Common:9; Rare:438; Clinvar (pathogenic):2 | ||||
| chr19:12696060-12696330 | Common:6; Rare:106 | ||||
| chr19:12696524-12696761 | Rare:242 | ||||
| chr19:12722188-12722369 | Rare:63 | ||||
| chr19:12722480-12722899 | Common:9; Rare:182 | ||||
| chr19:12723865-12724055 | Common:2; Rare:92 | ||||
| chr19:12734503-12734908 | Common:3; Rare:387 | ||||
| chr19:12736793-12737140 | Common:3; Rare:159 | ||||
| chr19:12737252-12737578 | Rare:83 | ||||
| chr19:12774940-12775376 | Common:10; Rare:206 | ||||
| chr19:12775454-12775806 | Common:9; Rare:270 |