| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:66751569-66752002 | Common:4; Rare:119 | ||||
| chr16:66830889-66831120 | Rare:101 | ||||
| chr16:66873205-66873605 | Common:6; Rare:148 | ||||
| chr16:66880324-66880646 | Common:2; Rare:78 | ||||
| chr16:66934357-66934533 | Common:1; Rare:67 | ||||
| chr16:66961020-66961270 | Common:2; Rare:51 | ||||
| chr16:67028441-67028841 | Common:2; Rare:95 | ||||
| chr16:67028859-67029332 | Common:4; Rare:168 | ||||
| chr16:67029760-67030160 | Rare:130 | ||||
| chr16:67093444-67093628 | Common:1; Rare:31 | ||||
| chr16:67109757-67109999 | Rare:81 | ||||
| chr16:67150730-67151250 | Common:2; Rare:132 | ||||
| chr16:67163064-67163464 | Common:3; Rare:189; Clinvar (benign):1 | ||||
| chr16:67163470-67163940 | Common:2; Rare:172; Clinvar:2; Clinvar (benign):3 | ||||
| chr16:67170360-67170600 | Common:1; Rare:41 |