| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:127823116-127823364 | Common:3; Rare:55 | ||||
| chr3:128052173-128052525 | Common:2; Rare:120 | ||||
| chr3:128123758-128123984 | Rare:59 | ||||
| chr3:128153356-128153518 | Rare:48 | ||||
| chr3:128487892-128488064 | Common:1; Rare:45 | ||||
| chr3:128488351-128488640 | Common:1; Rare:59 | ||||
| chr3:128650756-128651167 | Common:2; Rare:109 | ||||
| chr3:128879391-128879724 | Common:4; Rare:160; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr3:128991426-128991668 | Rare:50 | ||||
| chr3:129001232-129001312 | Common:1; Rare:18 | ||||
| chr3:129161004-129161152 | Common:1; Rare:60 | ||||
| chr3:129161260-129161464 | Common:1; Rare:61 | ||||
| chr3:129183778-129184075 | Common:2; Rare:101 | ||||
| chr3:129249492-129249675 | Common:3; Rare:55 | ||||
| chr3:129260268-129260400 | Rare:45 |