| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:47164069-47164479 | Common:1; Rare:99 | ||||
| chr3:47380812-47381066 | Rare:77 | ||||
| chr3:47475776-47476080 | Common:3; Rare:116 | ||||
| chr3:47781814-47782048 | Rare:93 | ||||
| chr3:48301365-48301533 | Common:2; Rare:46 | ||||
| chr3:48440039-48440315 | Common:1; Rare:104 | ||||
| chr3:48473015-48473280 | Common:2; Rare:56 | ||||
| chr3:48847802-48847965 | Rare:52 | ||||
| chr3:48918733-48918984 | Common:2; Rare:135 | ||||
| chr3:48989763-48989892 | Rare:32 | ||||
| chr3:49007030-49007444 | Common:2; Rare:149 | ||||
| chr3:49020276-49020473 | Common:1; Rare:32 | ||||
| chr3:49021503-49021738 | Rare:56; Clinvar:1 | ||||
| chr3:49022011-49022154 | Rare:47; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr3:49024929-49025268 | Rare:92 |