| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:752953-753413 | Common:8; Rare:260; Clinvar:8; Clinvar (benign):13 | ||||
| chr12:949395-949868 | Common:12; Rare:258 | ||||
| chr12:990180-990586 | Common:5; Rare:160 | ||||
| chr12:990633-991427 | Common:24; Rare:670 | ||||
| chr12:1593466-1594010 | Common:7; Rare:261 | ||||
| chr12:1594113-1594421 | Common:5; Rare:169 | ||||
| chr12:1594389-1594889 | Common:1; Rare:285 | ||||
| chr12:1629440-1629710 | Common:3; Rare:49 | ||||
| chr12:1629730-1629990 | Common:2; Rare:48 | ||||
| chr12:1630230-1630860 | Common:8; Rare:137 | ||||
| chr12:1690793-1691266 | Common:10; Rare:412 | ||||
| chr12:1691450-1692092 | Common:3; Rare:183 | ||||
| chr12:1795861-1796400 | Common:7; Rare:242 | ||||
| chr12:2003785-2004025 | Common:3; Rare:44 | ||||
| chr12:2004000-2004340 | Common:6; Rare:181 |