| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:44976126-44976280 | Common:2; Rare:66 | ||||
| chr3:48301353-48301480 | Common:1; Rare:35 | ||||
| chr3:48440056-48440303 | Common:1; Rare:92 | ||||
| chr3:48918783-48918874 | Common:2; Rare:53 | ||||
| chr3:49021993-49022157 | Rare:54; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr3:49133020-49133105 | Rare:19 | ||||
| chr3:50328180-50328342 | Rare:47 | ||||
| chr3:51385064-51385338 | Common:2; Rare:83 | ||||
| chr3:52239089-52239255 | Common:2; Rare:61 | ||||
| chr3:52685960-52686032 | Common:1; Rare:23 | ||||
| chr3:52705776-52706181 | Common:2; Rare:142 | ||||
| chr3:53891849-53892035 | Common:1; Rare:48 | ||||
| chr3:57597338-57597674 | Common:4; Rare:108 | ||||
| chr3:62318890-62319068 | Rare:73 | ||||
| chr3:67654592-67654655 | Rare:24 |