| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:56843606-56843939 | Common:18; Rare:136 | ||||
| chr6:56954704-56955540 | Common:6; Rare:358 | ||||
| chr6:57046462-57046768 | Rare:201 | ||||
| chr6:57089885-57090258 | Rare:140 | ||||
| chr6:57172132-57172377 | Rare:116 | ||||
| chr6:57172519-57172773 | Common:2; Rare:155 | ||||
| chr6:57317514-57317674 | Rare:85 | ||||
| chr6:63572190-63572691 | Rare:325 | ||||
| chr6:63573541-63573798 | Rare:124 | ||||
| chr6:63635667-63636038 | Common:2; Rare:226 | ||||
| chr6:63636040-63636327 | Common:1; Rare:89 | ||||
| chr6:69796869-69797140 | Common:1; Rare:158; Clinvar:8; Clinvar (benign):3 | ||||
| chr6:70413149-70413624 | Common:4; Rare:275 | ||||
| chr6:70667684-70668001 | Common:6; Rare:214 | ||||
| chr6:73461677-73461981 | Common:2; Rare:144; Clinvar:2; Clinvar (benign):3 |