| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:133491065-133491236 | Rare:40 | ||||
| chr3:134537070-134537207 | Rare:28; Clinvar (pathogenic):1 | ||||
| chr3:139361084-139361454 | Rare:69 | ||||
| chr3:141311708-141311871 | Common:1; Rare:45 | ||||
| chr3:141660104-141660346 | Rare:65 | ||||
| chr3:142445999-142446165 | Rare:27 | ||||
| chr3:143082251-143082561 | Rare:56 | ||||
| chr3:143120056-143120241 | Rare:46 | ||||
| chr3:143494832-143495059 | Common:1; Rare:42 | ||||
| chr3:146533513-146533614 | Rare:32 | ||||
| chr3:146542354-146542503 | Rare:25 | ||||
| chr3:149185382-149185677 | Common:6; Rare:61 | ||||
| chr3:150226092-150226346 | Common:1; Rare:54 | ||||
| chr3:150408855-150409187 | Rare:83 | ||||
| chr3:150890405-150890659 | Rare:42 |