| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:43687757-43687860 | Common:1; Rare:42 | ||||
| chr6:43770070-43770230 | Common:2; Rare:48 | ||||
| chr6:43771906-43771980 | Rare:16 | ||||
| chr6:44127351-44127639 | Common:4; Rare:81 | ||||
| chr6:44219502-44219699 | Common:2; Rare:55 | ||||
| chr6:44223459-44223637 | Common:1; Rare:56 | ||||
| chr6:44246896-44247192 | Common:4; Rare:123 | ||||
| chr6:44387445-44387774 | Common:4; Rare:87 | ||||
| chr6:45377792-45378209 | Common:2; Rare:133 | ||||
| chr6:46129843-46129993 | Common:1; Rare:37 | ||||
| chr6:46652676-46653022 | Rare:83 | ||||
| chr6:46921922-46922080 | Rare:39 | ||||
| chr6:47042330-47042452 | Common:1; Rare:30 | ||||
| chr6:47477683-47478015 | Common:2; Rare:87; Clinvar:3; Clinvar (benign):3 | ||||
| chr6:49463174-49463397 | Common:1; Rare:67; Clinvar:1; Clinvar (benign):1 |