| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:125520039-125520405 | Rare:114 | ||||
| chr3:126083986-126084171 | Common:2; Rare:50 | ||||
| chr3:127598208-127598449 | Common:3; Rare:66 | ||||
| chr3:127672805-127673011 | Common:3; Rare:99 | ||||
| chr3:128052175-128052562 | Common:2; Rare:133 | ||||
| chr3:128123793-128123967 | Rare:37 | ||||
| chr3:128153371-128153487 | Rare:32 | ||||
| chr3:128487917-128488052 | Rare:32 | ||||
| chr3:128879423-128879685 | Common:4; Rare:130; Clinvar:2; Clinvar (benign):3 | ||||
| chr3:129183822-129184074 | Common:2; Rare:86 | ||||
| chr3:129249495-129249744 | Common:3; Rare:70 | ||||
| chr3:129439753-129440358 | Common:1; Rare:182; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:129560529-129560652 | Rare:24 | ||||
| chr3:129893594-129893870 | Rare:124 | ||||
| chr3:130893916-130894244 | Common:3; Rare:95 |