| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:15911550-15911685 | Rare:26 | ||||
| chr12:16347471-16347727 | Common:4; Rare:50 | ||||
| chr12:16606616-16606652 | Rare:5 | ||||
| chr12:19439331-19439743 | Common:3; Rare:153 | ||||
| chr12:19440116-19440704 | Common:2; Rare:206 | ||||
| chr12:21437531-21437603 | Common:2; Rare:14 | ||||
| chr12:21437605-21437995 | Common:6; Rare:165 | ||||
| chr12:21501249-21501444 | Common:1; Rare:48 | ||||
| chr12:21501516-21501933 | Common:6; Rare:121 | ||||
| chr12:21502291-21502364 | Rare:16 | ||||
| chr12:21527454-21527579 | Common:1; Rare:31 | ||||
| chr12:21527779-21528133 | Common:2; Rare:105 | ||||
| chr12:21656976-21657128 | Common:1; Rare:34 | ||||
| chr12:21657711-21658098 | Common:4; Rare:110; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:21774453-21774561 | Rare:29; Clinvar (benign):1 |