| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:32838172-32838302 | Common:1; Rare:38; Clinvar (benign):2 | ||||
| chr6:32838705-32839090 | Common:7; Rare:57 | ||||
| chr6:32843915-32844126 | Common:1; Rare:57; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:32844300-32844848 | Common:1; Rare:121 | ||||
| chr6:32853665-32853777 | Common:1; Rare:48; Clinvar:2; Clinvar (benign):2 | ||||
| chr6:32853979-32854237 | Common:2; Rare:61 | ||||
| chr6:32969086-32969384 | Common:5; Rare:85 | ||||
| chr6:32969536-32969571 | Rare:11 | ||||
| chr6:32970643-32970952 | Common:2; Rare:83 | ||||
| chr6:32976396-32976655 | Rare:105 | ||||
| chr6:33200356-33200449 | Rare:24 | ||||
| chr6:33200656-33200937 | Common:2; Rare:85 | ||||
| chr6:33208439-33208524 | Rare:22 | ||||
| chr6:33271632-33272166 | Common:4; Rare:190 | ||||
| chr6:33275617-33275883 | Common:1; Rare:59 |