| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:32223973-32224190 | Common:1; Rare:41 | ||||
| chr6:32530239-32530480 | Common:17; Rare:20 | ||||
| chr6:32666636-32666926 | Common:45; Rare:25 | ||||
| chr6:32844001-32844126 | Rare:27; Clinvar:1 | ||||
| chr6:32844328-32844848 | Common:1; Rare:114 | ||||
| chr6:32853664-32853799 | Common:1; Rare:63; Clinvar:2; Clinvar (benign):2 | ||||
| chr6:32853989-32854227 | Common:2; Rare:56 | ||||
| chr6:32968502-32968607 | Common:1; Rare:28 | ||||
| chr6:32968819-32968933 | Common:4; Rare:34 | ||||
| chr6:32969068-32969352 | Common:5; Rare:86 | ||||
| chr6:32970154-32970267 | Common:1; Rare:28 | ||||
| chr6:32970802-32970970 | Common:1; Rare:46 | ||||
| chr6:33075795-33076036 | Common:3; Rare:30 | ||||
| chr6:33200356-33200445 | Rare:22 | ||||
| chr6:33200654-33200938 | Common:2; Rare:85 |