| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:34991282-34991344 | Rare:15 | ||||
| chr9:35079990-35080107 | Common:3; Rare:29; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:35103082-35103157 | Common:1; Rare:38 | ||||
| chr9:35103166-35103279 | Rare:27 | ||||
| chr9:35489810-35490148 | Common:3; Rare:108 | ||||
| chr9:35657865-35658385 | Common:7; Rare:431; Clinvar:38; Clinvar (benign):14; Clinvar (pathogenic):40 | ||||
| chr9:35689783-35690111 | Common:4; Rare:109; Clinvar:4; Clinvar (benign):1 | ||||
| chr9:35732094-35732677 | Common:4; Rare:165 | ||||
| chr9:35748946-35749361 | Common:2; Rare:150 | ||||
| chr9:35812143-35812272 | Rare:50 | ||||
| chr9:35814983-35815314 | Rare:84 | ||||
| chr9:36190738-36190994 | Common:1; Rare:86 | ||||
| chr9:36258385-36258625 | Common:2; Rare:55; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:37120193-37120618 | Common:2; Rare:132 | ||||
| chr9:37422631-37422755 | Common:2; Rare:68 |