| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:109154400-109154800 | Common:5; Rare:236 | ||||
| chr12:109154841-109155355 | Common:6; Rare:215 | ||||
| chr12:109477174-109477714 | Common:23; Rare:690 | ||||
| chr12:109573039-109573443 | Common:13; Rare:254; Clinvar:4; Clinvar (benign):4 | ||||
| chr12:109573396-109573869 | Common:23; Rare:859; Clinvar:40; Clinvar (benign):39; Clinvar (pathogenic):10 | ||||
| chr12:109880314-109880832 | Common:10; Rare:732 | ||||
| chr12:109900123-109900703 | Rare:553 | ||||
| chr12:109901045-109901488 | Common:5; Rare:151 | ||||
| chr12:109995566-109996069 | Common:4; Rare:177 | ||||
| chr12:109996150-109996670 | Common:11; Rare:394 | ||||
| chr12:109998553-109999500 | Rare:556 | ||||
| chr12:110048354-110048790 | Common:7; Rare:339 | ||||
| chr12:110124056-110124474 | Common:5; Rare:346 | ||||
| chr12:110124483-110124883 | Common:2; Rare:65 | ||||
| chr12:110280361-110280761 | Rare:130 |