| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:33317946-33318152 | Common:1; Rare:51 | ||||
| chr6:33320045-33320464 | Common:2; Rare:135; Clinvar (pathogenic):1 | ||||
| chr6:33322675-33323310 | Common:6; Rare:186 | ||||
| chr6:33391516-33391922 | Common:3; Rare:97 | ||||
| chr6:33406603-33406874 | Rare:71 | ||||
| chr6:33410022-33410608 | Common:2; Rare:146 | ||||
| chr6:33417714-33418514 | Common:4; Rare:216 | ||||
| chr6:33419770-33419928 | Common:1; Rare:20 | ||||
| chr6:33420040-33420319 | Rare:56; Clinvar (benign):1 | ||||
| chr6:33420333-33420555 | Common:1; Rare:33; Clinvar (benign):1 | ||||
| chr6:33431411-33431618 | Rare:35 | ||||
| chr6:33431780-33432395 | Common:4; Rare:133; Clinvar (benign):4 | ||||
| chr6:33454446-33454692 | Rare:60 | ||||
| chr6:33620077-33620364 | Common:4; Rare:60 | ||||
| chr6:33711561-33711587 | Common:1; Rare:10; Clinvar (benign):1 |