| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:12715380-12715555 | Common:2; Rare:27 | ||||
| chr12:12716746-12716885 | Common:1; Rare:43 | ||||
| chr12:12716945-12717251 | Common:2; Rare:99 | ||||
| chr12:12717254-12717636 | Common:1; Rare:120; Clinvar:3; Clinvar (benign):3 | ||||
| chr12:12718189-12718261 | Rare:29; Clinvar:6; Clinvar (benign):7 | ||||
| chr12:12725021-12725605 | Common:5; Rare:141 | ||||
| chr12:12725618-12726052 | Common:5; Rare:110 | ||||
| chr12:12726062-12726135 | Common:1; Rare:16 | ||||
| chr12:12813219-12813450 | Common:1; Rare:68 | ||||
| chr12:12820081-12820263 | Common:1; Rare:28 | ||||
| chr12:12890590-12890712 | Rare:22 | ||||
| chr12:12890717-12890795 | Rare:11 | ||||
| chr12:12890803-12891044 | Rare:48 | ||||
| chr12:12891197-12891334 | Common:1; Rare:33 | ||||
| chr12:12891337-12891642 | Common:1; Rare:57 |