| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:41200386-41200471 | Common:2; Rare:17 | ||||
| chr3:41962015-41962562 | Common:8; Rare:136 | ||||
| chr3:42091041-42091395 | Rare:59 | ||||
| chr3:42160063-42160221 | Common:1; Rare:33 | ||||
| chr3:42192584-42192758 | Common:3; Rare:27 | ||||
| chr3:42581913-42582188 | Common:3; Rare:82 | ||||
| chr3:42600328-42600778 | Common:3; Rare:174 | ||||
| chr3:42773236-42773345 | Common:1; Rare:27 | ||||
| chr3:42804242-42804663 | Common:2; Rare:113 | ||||
| chr3:42936335-42936425 | Common:1; Rare:28 | ||||
| chr3:43286449-43286619 | Common:1; Rare:80 | ||||
| chr3:43621914-43622316 | Common:2; Rare:118; Clinvar:7; Clinvar (benign):1 | ||||
| chr3:43690747-43691013 | Common:5; Rare:142; Clinvar:7; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr3:44338086-44338193 | Common:2; Rare:38 | ||||
| chr3:44338397-44338799 | Common:6; Rare:133 |