| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:109691135-109691375 | Common:3; Rare:58; Clinvar:5; Clinvar (benign):3 | ||||
| chr6:110179866-110180170 | Common:2; Rare:82 | ||||
| chr6:110958392-110958463 | Common:1; Rare:15 | ||||
| chr6:110958466-110958609 | Common:3; Rare:36 | ||||
| chr6:110958617-110958788 | Common:4; Rare:66 | ||||
| chr6:110981963-110982113 | Common:2; Rare:77 | ||||
| chr6:111259191-111259387 | Common:2; Rare:68 | ||||
| chr6:111483208-111483775 | Common:2; Rare:207 | ||||
| chr6:111567139-111567205 | Rare:15 | ||||
| chr6:111573634-111573717 | Common:1; Rare:11 | ||||
| chr6:111573731-111573794 | Common:1; Rare:9 | ||||
| chr6:111873417-111873625 | Common:1; Rare:75 | ||||
| chr6:112087352-112087707 | Common:1; Rare:113 | ||||
| chr6:113857251-113857445 | Common:1; Rare:42 | ||||
| chr6:113970318-113970388 | Rare:22 |