| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:149215722-149215772 | Rare:3 | ||||
| chr3:149224038-149224268 | Common:4; Rare:36 | ||||
| chr3:149376965-149377038 | Rare:14 | ||||
| chr3:149392096-149392133 | Common:1; Rare:6 | ||||
| chr3:150252583-150252628 | Rare:7 | ||||
| chr3:150408860-150408998 | Rare:39 | ||||
| chr3:150770812-150771148 | Common:1; Rare:51 | ||||
| chr3:151770162-151770488 | Common:3; Rare:54 | ||||
| chr3:154140111-154140274 | Common:1; Rare:26 | ||||
| chr3:154255166-154255395 | Common:1; Rare:72 | ||||
| chr3:156816979-156817248 | Rare:86 | ||||
| chr3:157174857-157175022 | Common:3; Rare:72 | ||||
| chr3:158691260-158691419 | Common:1; Rare:56; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:169765044-169765215 | Rare:75; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr3:177211660-177211872 | Common:1; Rare:27 |