| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:40524808-40525013 | Common:1; Rare:59 | ||||
| chr3:42581903-42582137 | Common:3; Rare:72 | ||||
| chr3:42600343-42600778 | Common:3; Rare:168 | ||||
| chr3:42804256-42804677 | Common:2; Rare:116 | ||||
| chr3:43621907-43622342 | Common:2; Rare:127; Clinvar:7; Clinvar (benign):1 | ||||
| chr3:43690641-43691004 | Common:6; Rare:161; Clinvar:7; Clinvar (benign):2 | ||||
| chr3:44338319-44338527 | Common:3; Rare:73 | ||||
| chr3:44338698-44338797 | Common:3; Rare:37 | ||||
| chr3:44477646-44477736 | Common:1; Rare:17 | ||||
| chr3:44624913-44625085 | Common:2; Rare:51 | ||||
| chr3:44729524-44729667 | Common:1; Rare:55 | ||||
| chr3:44761518-44761809 | Common:3; Rare:124 | ||||
| chr3:44861815-44861927 | Common:2; Rare:55 | ||||
| chr3:44976028-44976287 | Common:4; Rare:100 | ||||
| chr3:45146207-45146525 | Common:2; Rare:107 |