| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:196503689-196503952 | Common:5; Rare:91 | ||||
| chr3:196639608-196639812 | Common:2; Rare:47 | ||||
| chr3:196712208-196712581 | Common:6; Rare:120 | ||||
| chr3:196942388-196942659 | Common:1; Rare:109 | ||||
| chr3:197949890-197950250 | Common:4; Rare:111; Clinvar (benign):2 | ||||
| chr3:197950825-197950978 | Rare:37; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:197959960-197960244 | Common:1; Rare:100 | ||||
| chr4:305455-305643 | Common:2; Rare:57 | ||||
| chr4:337492-337879 | Common:3; Rare:109 | ||||
| chr4:499136-499279 | Common:3; Rare:48 | ||||
| chr4:663616-663723 | Rare:35 | ||||
| chr4:674212-674558 | Common:2; Rare:159 | ||||
| chr4:677629-678029 | Common:1; Rare:90 | ||||
| chr4:678323-678618 | Common:6; Rare:75 | ||||
| chr4:681200-681235 | Rare:13 |