| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:33718068-33718275 | Rare:70 | ||||
| chr3:33798512-33798929 | Common:3; Rare:150 | ||||
| chr3:36993078-36993564 | Common:2; Rare:166; Clinvar:27; Clinvar (benign):12; Clinvar (pathogenic):3 | ||||
| chr3:37176077-37176389 | Common:1; Rare:86 | ||||
| chr3:37861711-37861963 | Common:1; Rare:54 | ||||
| chr3:39107568-39107732 | Common:4; Rare:50 | ||||
| chr3:40309506-40309808 | Common:8; Rare:107 | ||||
| chr3:41199782-41200165 | Common:2; Rare:110 | ||||
| chr3:42581848-42582148 | Common:4; Rare:93 | ||||
| chr3:42582242-42582626 | Common:3; Rare:76 | ||||
| chr3:42600496-42600689 | Common:1; Rare:78 | ||||
| chr3:42804435-42804570 | Common:1; Rare:44 | ||||
| chr3:44624832-44625056 | Common:1; Rare:56 | ||||
| chr3:44625475-44625538 | Rare:14 | ||||
| chr3:44761613-44761807 | Common:2; Rare:66 |