| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:42581898-42582123 | Common:2; Rare:72 | ||||
| chr3:42600410-42600766 | Common:2; Rare:130 | ||||
| chr3:42600865-42601009 | Rare:55 | ||||
| chr3:42630827-42631143 | Common:1; Rare:59 | ||||
| chr3:42635105-42635140 | Rare:6 | ||||
| chr3:42773211-42773345 | Common:1; Rare:38 | ||||
| chr3:42804394-42804657 | Common:2; Rare:77 | ||||
| chr3:43286449-43286654 | Common:2; Rare:91 | ||||
| chr3:43621919-43622312 | Common:2; Rare:115; Clinvar:7; Clinvar (benign):1 | ||||
| chr3:43690616-43690962 | Common:4; Rare:130; Clinvar:5; Clinvar (benign):1 | ||||
| chr3:44477655-44477752 | Common:1; Rare:15 | ||||
| chr3:44761559-44761794 | Common:3; Rare:97 | ||||
| chr3:44861763-44861918 | Common:2; Rare:69 | ||||
| chr3:44976100-44976280 | Common:2; Rare:71 | ||||
| chr3:45146340-45146509 | Common:1; Rare:55 |