| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:42804453-42804646 | Common:2; Rare:55 | ||||
| chr3:43621890-43622322 | Common:2; Rare:124; Clinvar:7; Clinvar (benign):1 | ||||
| chr3:44338707-44338799 | Common:3; Rare:32 | ||||
| chr3:44477637-44477799 | Common:1; Rare:34 | ||||
| chr3:44624935-44625095 | Common:2; Rare:45 | ||||
| chr3:44861808-44861922 | Common:2; Rare:55 | ||||
| chr3:44976112-44976304 | Common:3; Rare:82 | ||||
| chr3:47164061-47164244 | Rare:43 | ||||
| chr3:47380832-47381066 | Rare:65 | ||||
| chr3:47475816-47476068 | Common:3; Rare:105 | ||||
| chr3:48301362-48301483 | Common:1; Rare:28 | ||||
| chr3:48440031-48440270 | Common:1; Rare:73 | ||||
| chr3:48918813-48918935 | Common:2; Rare:75 | ||||
| chr3:48989721-48989932 | Rare:53 | ||||
| chr3:49007032-49007429 | Common:2; Rare:139 |