| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:2004403-2004629 | Common:1; Rare:90 | ||||
| chr12:2812489-2812737 | Common:1; Rare:64 | ||||
| chr12:2812880-2813029 | Rare:44 | ||||
| chr12:2877015-2877268 | Rare:79 | ||||
| chr12:2959848-2959958 | Common:1; Rare:28 | ||||
| chr12:4275455-4275703 | Common:3; Rare:45 | ||||
| chr12:4320949-4321260 | Common:5; Rare:118 | ||||
| chr12:4538444-4538907 | Common:1; Rare:102 | ||||
| chr12:4648965-4649170 | Common:2; Rare:68; Clinvar (benign):2 | ||||
| chr12:6375374-6375569 | Common:2; Rare:48; Clinvar:1; Clinvar (benign):3 | ||||
| chr12:6376235-6376449 | Common:2; Rare:43 | ||||
| chr12:6451780-6452120 | Common:4; Rare:62 | ||||
| chr12:6493230-6493394 | Common:6; Rare:46 | ||||
| chr12:6493767-6494140 | Common:2; Rare:110 | ||||
| chr12:6568224-6568393 | Rare:63 |