| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:64609132-64609272 | Common:1; Rare:21 | ||||
| chr12:64611136-64611176 | Rare:10 | ||||
| chr12:64625310-64625530 | Common:1; Rare:35 | ||||
| chr12:64625729-64625921 | Common:1; Rare:44 | ||||
| chr12:64669205-64669511 | Common:3; Rare:54 | ||||
| chr12:64671418-64671503 | Rare:13 | ||||
| chr12:64779285-64779570 | Rare:35 | ||||
| chr12:64818425-64818562 | Rare:25 | ||||
| chr12:64889882-64890211 | Rare:53 | ||||
| chr12:64890805-64890820 | Rare:2 | ||||
| chr12:64998561-64998796 | Common:1; Rare:25 | ||||
| chr12:65170118-65170177 | Rare:18 | ||||
| chr12:65170416-65170528 | Rare:53; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:65170546-65170615 | Rare:23 | ||||
| chr12:65533319-65533460 | Common:1; Rare:29 |