| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:49022009-49022141 | Rare:40; Clinvar:2 | ||||
| chr3:49029357-49029467 | Common:1; Rare:80 | ||||
| chr3:49104692-49104919 | Common:1; Rare:98; Clinvar:1; Clinvar (benign):5 | ||||
| chr3:49132969-49133125 | Rare:35; Clinvar:2 | ||||
| chr3:49411839-49412213 | Common:1; Rare:124 | ||||
| chr3:49674228-49674404 | Common:1; Rare:70 | ||||
| chr3:49689460-49689606 | Rare:46 | ||||
| chr3:49903854-49903984 | Rare:40 | ||||
| chr3:50292336-50292626 | Common:1; Rare:123 | ||||
| chr3:50328167-50328339 | Rare:55 | ||||
| chr3:50350697-50350886 | Common:1; Rare:28 | ||||
| chr3:50359382-50359592 | Common:2; Rare:60 | ||||
| chr3:50365200-50365379 | Common:1; Rare:69 | ||||
| chr3:50611728-50612088 | Common:2; Rare:85; Clinvar:1 | ||||
| chr3:50617412-50617559 | Common:1; Rare:21 |