| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:43687757-43687960 | Common:2; Rare:65 | ||||
| chr6:43770087-43770539 | Common:5; Rare:107 | ||||
| chr6:43770734-43770929 | Common:1; Rare:59 | ||||
| chr6:43771670-43771990 | Common:4; Rare:58 | ||||
| chr6:44126525-44126650 | Common:1; Rare:27 | ||||
| chr6:44126691-44126919 | Rare:56 | ||||
| chr6:44127358-44127663 | Common:4; Rare:88 | ||||
| chr6:46129774-46130166 | Common:5; Rare:125 | ||||
| chr6:47477643-47478255 | Common:5; Rare:178; Clinvar:7; Clinvar (benign):7 | ||||
| chr6:49463166-49463393 | Common:1; Rare:67; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:52362031-52362204 | Common:2; Rare:54 | ||||
| chr6:52362626-52362705 | Rare:15 | ||||
| chr6:52420150-52420356 | Common:3; Rare:86; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:52577349-52577466 | Common:1; Rare:39 | ||||
| chr6:52995267-52995841 | Common:4; Rare:236 |