| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:127672805-127673011 | Common:3; Rare:99 | ||||
| chr3:127791223-127791323 | Common:1; Rare:12 | ||||
| chr3:127822349-127822416 | Rare:16 | ||||
| chr3:127823128-127823553 | Common:4; Rare:93 | ||||
| chr3:128051569-128051653 | Rare:15 | ||||
| chr3:128052173-128052902 | Common:3; Rare:241 | ||||
| chr3:128123740-128124008 | Rare:77 | ||||
| chr3:128153373-128153496 | Rare:35 | ||||
| chr3:128650541-128650627 | Rare:30 | ||||
| chr3:128726273-128726356 | Common:1; Rare:19; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:128879401-128879783 | Common:4; Rare:190; Clinvar:5; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr3:128897617-128897644 | Rare:8; Clinvar:1 | ||||
| chr3:129121476-129121937 | Common:4; Rare:109 | ||||
| chr3:129160982-129161147 | Common:1; Rare:65 | ||||
| chr3:129183745-129184084 | Common:3; Rare:114 |