| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:73625591-73626185 | Rare:170 | ||||
| chr10:73744234-73744457 | Common:2; Rare:110 | ||||
| chr10:73772194-73772328 | Common:2; Rare:56 | ||||
| chr10:73772414-73772708 | Rare:197 | ||||
| chr10:73772856-73773204 | Common:2; Rare:195 | ||||
| chr10:73781937-73782352 | Common:2; Rare:195 | ||||
| chr10:73785538-73785677 | Rare:77 | ||||
| chr10:73874473-73874739 | Rare:135 | ||||
| chr10:73874920-73875230 | Rare:112 | ||||
| chr10:73909034-73909222 | Rare:42 | ||||
| chr10:73997793-73998307 | Common:3; Rare:210; Clinvar:2; Clinvar (benign):3 | ||||
| chr10:74150662-74150853 | Common:3; Rare:36 | ||||
| chr10:74151034-74151291 | Common:2; Rare:142 | ||||
| chr10:74176410-74176885 | Common:1; Rare:226; Clinvar:6; Clinvar (benign):1 | ||||
| chr10:74177050-74177300 | Common:2; Rare:73 |