| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:187744604-187745004 | Common:6; Rare:266 | ||||
| chr3:187745282-187745953 | Common:2; Rare:580 | ||||
| chr3:190513820-190514110 | Common:5; Rare:133 | ||||
| chr3:191329090-191330225 | Common:40; Rare:781; Clinvar (benign):2 | ||||
| chr3:193240929-193241350 | Common:18; Rare:605 | ||||
| chr3:193592830-193593394 | Rare:711; Clinvar:10; Clinvar (benign):6 | ||||
| chr3:193593424-193594190 | Common:4; Rare:308 | ||||
| chr3:193662400-193663105 | Common:1; Rare:162; Clinvar:7; Clinvar (benign):2 | ||||
| chr3:194135877-194136246 | Rare:280 | ||||
| chr3:194486824-194487268 | Common:31; Rare:837 | ||||
| chr3:194632480-194633032 | Common:5; Rare:172 | ||||
| chr3:194633043-194634210 | Common:46; Rare:741 | ||||
| chr3:194671951-194672731 | Common:33; Rare:1154 | ||||
| chr3:195154006-195155070 | Common:5; Rare:270 | ||||
| chr3:195184922-195185322 | Common:13; Rare:69 |