| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:47475804-47476068 | Common:3; Rare:107 | ||||
| chr3:47513672-47513788 | Rare:34 | ||||
| chr3:48088784-48089059 | Rare:89 | ||||
| chr3:48440027-48440312 | Common:1; Rare:107 | ||||
| chr3:48473010-48473251 | Common:1; Rare:55 | ||||
| chr3:48504060-48504281 | Common:2; Rare:69 | ||||
| chr3:48556789-48557173 | Common:1; Rare:86 | ||||
| chr3:48918815-48918912 | Common:2; Rare:57 | ||||
| chr3:49007192-49007424 | Common:2; Rare:92 | ||||
| chr3:49018552-49018649 | Rare:33 | ||||
| chr3:49021502-49021720 | Rare:55; Clinvar:1 | ||||
| chr3:49022010-49022162 | Rare:48; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr3:49025125-49025386 | Rare:57 | ||||
| chr3:49029378-49029458 | Common:1; Rare:54 | ||||
| chr3:49104720-49104959 | Rare:96; Clinvar:1; Clinvar (benign):4 |