| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:32755446-32755598 | Common:1; Rare:60; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr12:32755860-32756034 | Common:1; Rare:64 | ||||
| chr12:32896513-32897029 | Common:7; Rare:166; Clinvar:18; Clinvar (benign):17; Clinvar (pathogenic):3 | ||||
| chr12:39619804-39619919 | Common:1; Rare:21 | ||||
| chr12:40224995-40225060 | Common:1; Rare:17; Clinvar (benign):1 | ||||
| chr12:41188784-41188985 | Common:4; Rare:83 | ||||
| chr12:42238164-42238462 | Common:1; Rare:98 | ||||
| chr12:42325964-42326213 | Common:1; Rare:79 | ||||
| chr12:42483910-42484172 | Common:1; Rare:37 | ||||
| chr12:42589234-42589456 | Common:2; Rare:40; Clinvar (benign):1 | ||||
| chr12:42589678-42589879 | Common:1; Rare:82; Clinvar:2 | ||||
| chr12:43806236-43806427 | Common:2; Rare:67 | ||||
| chr12:45215728-45215867 | Rare:25 | ||||
| chr12:45215976-45216300 | Common:1; Rare:98 | ||||
| chr12:45729559-45729747 | Rare:56 |