| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:42906666-42906935 | Rare:41 | ||||
| chr3:43286431-43286673 | Common:2; Rare:101 | ||||
| chr3:43621919-43622148 | Common:2; Rare:88; Clinvar:7; Clinvar (benign):1 | ||||
| chr3:43690613-43691023 | Common:7; Rare:177; Clinvar:8; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr3:43691560-43691768 | Common:2; Rare:44 | ||||
| chr3:44338330-44338527 | Common:3; Rare:70 | ||||
| chr3:44338667-44338797 | Common:3; Rare:47 | ||||
| chr3:44477646-44477745 | Common:1; Rare:18 | ||||
| chr3:44624860-44625095 | Common:2; Rare:69 | ||||
| chr3:44761577-44761809 | Common:3; Rare:89 | ||||
| chr3:44861803-44861927 | Common:2; Rare:59 | ||||
| chr3:44976069-44976326 | Common:3; Rare:106 | ||||
| chr3:45146207-45146332 | Common:1; Rare:42 | ||||
| chr3:45689156-45689463 | Common:2; Rare:105 | ||||
| chr3:45995739-45995868 | Rare:29; Clinvar:1 |