| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:752301-752615 | Common:1; Rare:96 | ||||
| chr12:990486-990586 | Common:1; Rare:31 | ||||
| chr12:991101-991316 | Common:3; Rare:98 | ||||
| chr12:2004403-2004473 | Rare:40 | ||||
| chr12:2004522-2004669 | Common:2; Rare:39 | ||||
| chr12:2812513-2812752 | Common:1; Rare:69 | ||||
| chr12:2877056-2877260 | Rare:62 | ||||
| chr12:3077249-3077439 | Common:7; Rare:83 | ||||
| chr12:4273583-4273803 | Rare:64 | ||||
| chr12:4320949-4321253 | Common:5; Rare:115 | ||||
| chr12:4538444-4538930 | Common:3; Rare:110 | ||||
| chr12:4649005-4649178 | Common:2; Rare:58; Clinvar (benign):2 | ||||
| chr12:5433236-5433372 | Common:1; Rare:32 | ||||
| chr12:6361897-6362035 | Common:1; Rare:37 | ||||
| chr12:6383976-6384452 | Common:2; Rare:118 |