| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:41224848-41224981 | Common:1; Rare:31; Clinvar (pathogenic):1 | ||||
| chr3:42013541-42013786 | Common:5; Rare:73 | ||||
| chr3:42160071-42160383 | Common:3; Rare:82 | ||||
| chr3:42581900-42582081 | Common:2; Rare:62 | ||||
| chr3:42582251-42582458 | Common:2; Rare:51 | ||||
| chr3:42600413-42600778 | Common:2; Rare:133 | ||||
| chr3:42773215-42773351 | Common:1; Rare:35 | ||||
| chr3:42804272-42804681 | Common:2; Rare:117 | ||||
| chr3:43286466-43286654 | Common:2; Rare:82 | ||||
| chr3:43690796-43690993 | Common:3; Rare:104; Clinvar:7; Clinvar (benign):2 | ||||
| chr3:43691556-43691594 | Common:1; Rare:8 | ||||
| chr3:44337853-44338167 | Common:2; Rare:79 | ||||
| chr3:44338706-44338797 | Common:3; Rare:32 | ||||
| chr3:44477655-44477959 | Common:1; Rare:48 | ||||
| chr3:44624935-44625095 | Common:2; Rare:45 |