| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:131381451-131381889 | Common:4; Rare:129 | ||||
| chr3:131502770-131503016 | Common:1; Rare:98 | ||||
| chr3:132317241-132317454 | Rare:44 | ||||
| chr3:132596985-132597275 | Common:1; Rare:38 | ||||
| chr3:132659756-132660005 | Common:3; Rare:57 | ||||
| chr3:132722066-132722225 | Common:1; Rare:66; Clinvar:11; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr3:133038184-133038419 | Common:1; Rare:80 | ||||
| chr3:133573567-133573690 | Common:1; Rare:42 | ||||
| chr3:133573824-133574045 | Rare:76 | ||||
| chr3:133574882-133575135 | Rare:71 | ||||
| chr3:133661789-133662024 | Rare:55 | ||||
| chr3:134029707-134030044 | Common:5; Rare:100 | ||||
| chr3:134030047-134030210 | Common:1; Rare:29 | ||||
| chr3:134373717-134373835 | Rare:35 | ||||
| chr3:134374369-134374669 | Common:2; Rare:86 |