| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:109900159-109900370 | Rare:71 | ||||
| chr12:109900878-109901173 | Common:1; Rare:60 | ||||
| chr12:109996204-109996479 | Common:2; Rare:82 | ||||
| chr12:109999028-109999482 | Rare:100 | ||||
| chr12:110048338-110048743 | Common:2; Rare:115 | ||||
| chr12:110124108-110124467 | Common:2; Rare:113 | ||||
| chr12:110280510-110280711 | Rare:52 | ||||
| chr12:110280916-110281341 | Common:1; Rare:159; Clinvar (benign):1 | ||||
| chr12:110281383-110281783 | Common:3; Rare:116; Clinvar:3; Clinvar (benign):6 | ||||
| chr12:110281927-110281966 | Rare:14 | ||||
| chr12:110281992-110282159 | Rare:54 | ||||
| chr12:110282169-110282394 | Common:1; Rare:50 | ||||
| chr12:110403172-110403285 | Rare:34 | ||||
| chr12:110403431-110403799 | Common:3; Rare:138 | ||||
| chr12:110404035-110404182 | Common:3; Rare:32 |