| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:7018350-7018710 | Common:2; Rare:106 | ||||
| chr12:7018763-7019049 | Common:3; Rare:77 | ||||
| chr12:7109225-7109375 | Rare:57 | ||||
| chr12:7130269-7130434 | Common:4; Rare:47 | ||||
| chr12:7189410-7189950 | Common:6; Rare:170; Clinvar:6; Clinvar (benign):2 | ||||
| chr12:8032743-8033143 | Common:6; Rare:165 | ||||
| chr12:8033059-8033801 | Common:4; Rare:210 | ||||
| chr12:8082068-8082316 | Common:2; Rare:83 | ||||
| chr12:8696931-8697336 | Common:6; Rare:176 | ||||
| chr12:8697778-8698033 | Common:1; Rare:109 | ||||
| chr12:8914274-8914388 | Common:1; Rare:28 | ||||
| chr12:8949593-8949710 | Rare:29 | ||||
| chr12:8949941-8950183 | Common:1; Rare:65 | ||||
| chr12:10212349-10212457 | Rare:27 | ||||
| chr12:10212650-10213050 | Common:8; Rare:158 |