| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:31715369-31715567 | Common:1; Rare:35 | ||||
| chr12:31728710-31729465 | Common:3; Rare:196 | ||||
| chr12:31959152-31959638 | Common:4; Rare:144 | ||||
| chr12:31959849-31959927 | Rare:15 | ||||
| chr12:31960063-31960264 | Rare:51 | ||||
| chr12:32106530-32107081 | Common:6; Rare:152 | ||||
| chr12:32679042-32679406 | Common:2; Rare:140; Clinvar:1; Clinvar (benign):4 | ||||
| chr12:32679623-32679794 | Rare:41 | ||||
| chr12:32755207-32755440 | Common:1; Rare:78; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr12:32755753-32756076 | Common:1; Rare:120; Clinvar (benign):1 | ||||
| chr12:34022152-34022540 | Common:3; Rare:92 | ||||
| chr12:38316438-38316835 | Common:9; Rare:99 | ||||
| chr12:38316936-38317074 | Common:1; Rare:54 | ||||
| chr12:38904905-38905349 | Rare:94 | ||||
| chr12:38905540-38906079 | Common:7; Rare:143 |