| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:184298935-184299338 | Common:5; Rare:121 | ||||
| chr3:184314435-184314673 | Common:3; Rare:69 | ||||
| chr3:184361606-184361770 | Rare:43 | ||||
| chr3:184711953-184712243 | Common:1; Rare:97 | ||||
| chr3:185254029-185254214 | Common:1; Rare:54 | ||||
| chr3:185282855-185283015 | Common:1; Rare:40 | ||||
| chr3:185498968-185499149 | Rare:64 | ||||
| chr3:185586154-185586358 | Common:1; Rare:49 | ||||
| chr3:186567291-186567454 | Common:3; Rare:41 | ||||
| chr3:186806402-186806542 | Rare:44 | ||||
| chr3:187139420-187139565 | Rare:55 | ||||
| chr3:188153649-188153938 | Common:1; Rare:59 | ||||
| chr3:190120362-190120570 | Rare:86; Clinvar (pathogenic):1 | ||||
| chr3:190322393-190322541 | Common:2; Rare:37 | ||||
| chr3:191329294-191329659 | Common:3; Rare:109 |