| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:168870650-168871219 | Rare:148 | ||||
| chr3:168877912-168878193 | Rare:68 | ||||
| chr3:168884320-168884720 | Rare:102 | ||||
| chr3:168888340-168888963 | Common:8; Rare:185 | ||||
| chr3:169183318-169183761 | Common:9; Rare:201 | ||||
| chr3:169321353-169321858 | Common:21; Rare:199 | ||||
| chr3:169534411-169534994 | Common:8; Rare:212 | ||||
| chr3:169613171-169613470 | Common:1; Rare:45 | ||||
| chr3:169624530-169625284 | Common:9; Rare:193 | ||||
| chr3:169627883-169628012 | Common:1; Rare:31 | ||||
| chr3:169634676-169635110 | Common:2; Rare:131 | ||||
| chr3:169657320-169657690 | Rare:76 | ||||
| chr3:169662104-169662542 | Common:7; Rare:151 | ||||
| chr3:169754730-169755050 | Common:1; Rare:52 | ||||
| chr3:169764288-169764890 | Common:3; Rare:205; Clinvar:22; Clinvar (benign):3; Clinvar (pathogenic):3 |