| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:41192827-41193065 | Rare:44 | ||||
| chr19:41193094-41193775 | Common:1; Rare:175 | ||||
| chr19:41193779-41194041 | Common:1; Rare:44 | ||||
| chr19:41218844-41219225 | Common:3; Rare:72 | ||||
| chr19:41262393-41262583 | Rare:32 | ||||
| chr19:41264983-41265401 | Common:2; Rare:93 | ||||
| chr19:41265549-41265764 | Common:1; Rare:36 | ||||
| chr19:41310114-41310301 | Rare:78 | ||||
| chr19:41310397-41310519 | Rare:27 | ||||
| chr19:41353589-41353669 | Rare:13 | ||||
| chr19:41364095-41364340 | Common:1; Rare:71; Clinvar:1 | ||||
| chr19:41397287-41397853 | Common:12; Rare:180; Clinvar (benign):5 | ||||
| chr19:41439503-41439652 | Rare:44 | ||||
| chr19:41860111-41860541 | Common:6; Rare:159; Clinvar:4; Clinvar (benign):2 | ||||
| chr19:41860894-41861152 | Common:2; Rare:74; Clinvar (benign):4 |