| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:401436-401664 | Rare:63 | ||||
| chr12:991088-991318 | Common:4; Rare:105 | ||||
| chr12:2004427-2004666 | Common:2; Rare:74 | ||||
| chr12:2877031-2877262 | Rare:70 | ||||
| chr12:4274194-4274235 | Rare:4 | ||||
| chr12:4320934-4321266 | Common:5; Rare:129 | ||||
| chr12:4538444-4538907 | Common:1; Rare:102 | ||||
| chr12:4649019-4649149 | Common:2; Rare:45; Clinvar (benign):1 | ||||
| chr12:6200005-6200559 | Common:4; Rare:166 | ||||
| chr12:6375346-6375667 | Common:3; Rare:83; Clinvar:1; Clinvar (benign):6 | ||||
| chr12:6383988-6384268 | Common:1; Rare:62 | ||||
| chr12:6451785-6452104 | Common:4; Rare:56 | ||||
| chr12:6493208-6493502 | Common:7; Rare:86 | ||||
| chr12:6493752-6494162 | Common:3; Rare:121 | ||||
| chr12:6534338-6534608 | Common:5; Rare:116 |