| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:48919213-48919864 | Common:3; Rare:198 | ||||
| chr3:48919821-48919955 | Rare:43 | ||||
| chr3:48989520-48990220 | Rare:440 | ||||
| chr3:49006870-49007740 | Common:12; Rare:896 | ||||
| chr3:49007700-49008307 | Common:12; Rare:519 | ||||
| chr3:49017440-49017810 | Rare:188 | ||||
| chr3:49017890-49018951 | Common:8; Rare:690 | ||||
| chr3:49020171-49020705 | Common:1; Rare:177 | ||||
| chr3:49020640-49020821 | Common:2; Rare:102 | ||||
| chr3:49020734-49021134 | Common:1; Rare:102 | ||||
| chr3:49021384-49021784 | Common:3; Rare:449; Clinvar:10; Clinvar (benign):2 | ||||
| chr3:49021890-49022185 | Rare:303; Clinvar:12; Clinvar (pathogenic):3 | ||||
| chr3:49022171-49022571 | Common:1; Rare:164; Clinvar:1; Clinvar (benign):5; Clinvar (pathogenic):3 | ||||
| chr3:49024359-49025351 | Common:3; Rare:634 | ||||
| chr3:49025348-49025941 | Common:2; Rare:129 |