| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:31959560-31959665 | Rare:29 | ||||
| chr12:31959785-31959920 | Rare:37 | ||||
| chr12:31960063-31960327 | Common:2; Rare:62 | ||||
| chr12:32106504-32107009 | Common:6; Rare:138 | ||||
| chr12:32107178-32107491 | Common:3; Rare:93 | ||||
| chr12:32399397-32399579 | Common:3; Rare:42 | ||||
| chr12:32399605-32399797 | Common:2; Rare:47 | ||||
| chr12:32501981-32502237 | Common:2; Rare:56; Clinvar:3; Clinvar (benign):2 | ||||
| chr12:32502405-32502643 | Rare:29 | ||||
| chr12:32679040-32679412 | Common:2; Rare:141; Clinvar:1; Clinvar (benign):4 | ||||
| chr12:32679524-32679966 | Common:5; Rare:106 | ||||
| chr12:32755775-32756091 | Common:1; Rare:109 | ||||
| chr12:32896761-32896875 | Common:1; Rare:39; Clinvar:4; Clinvar (benign):3 | ||||
| chr12:34022130-34022602 | Common:4; Rare:117 | ||||
| chr12:38316439-38316983 | Common:9; Rare:152 |