| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:43013869-43014329 | Common:2; Rare:101 | ||||
| chr6:43059808-43059880 | Rare:23 | ||||
| chr6:43182156-43182190 | Rare:5 | ||||
| chr6:43477488-43477605 | Rare:29 | ||||
| chr6:43516805-43517112 | Common:5; Rare:111; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:43575952-43576231 | Common:1; Rare:116; Clinvar:8 | ||||
| chr6:43687768-43687822 | Common:1; Rare:22 | ||||
| chr6:43769935-43770267 | Common:8; Rare:83 | ||||
| chr6:43770620-43770775 | Rare:41 | ||||
| chr6:44127278-44127639 | Common:4; Rare:97 | ||||
| chr6:44219496-44219645 | Rare:36 | ||||
| chr6:44387439-44387752 | Common:4; Rare:83 | ||||
| chr6:45377845-45378198 | Common:2; Rare:119 | ||||
| chr6:47477709-47478015 | Common:2; Rare:75; Clinvar:3; Clinvar (benign):3 | ||||
| chr6:47478133-47478260 | Common:1; Rare:49; Clinvar:1; Clinvar (benign):2 |