| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:40505945-40506132 | Rare:40 | ||||
| chr3:41962053-41962365 | Common:4; Rare:74 | ||||
| chr3:42149092-42149390 | Rare:70 | ||||
| chr3:42581913-42582137 | Common:3; Rare:69 | ||||
| chr3:42590693-42590903 | Common:3; Rare:61 | ||||
| chr3:42600328-42600709 | Common:3; Rare:152 | ||||
| chr3:42804434-42804657 | Common:2; Rare:66 | ||||
| chr3:43286434-43286654 | Common:2; Rare:97 | ||||
| chr3:43621924-43622316 | Common:2; Rare:113; Clinvar:7; Clinvar (benign):1 | ||||
| chr3:43690817-43690995 | Common:3; Rare:96; Clinvar:7; Clinvar (benign):2 | ||||
| chr3:44338667-44338797 | Common:3; Rare:47 | ||||
| chr3:44477625-44477758 | Common:1; Rare:29 | ||||
| chr3:44624839-44625090 | Common:2; Rare:70 | ||||
| chr3:44729521-44729687 | Common:1; Rare:63 | ||||
| chr3:44761577-44761809 | Common:3; Rare:89 |