| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:64464710-64464887 | Rare:34 | ||||
| chr12:64466258-64466506 | Common:2; Rare:38 | ||||
| chr12:64501246-64501435 | Common:1; Rare:65; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:64608974-64609034 | Rare:10 | ||||
| chr12:64619220-64619329 | Rare:17 | ||||
| chr12:64619882-64619972 | Rare:20 | ||||
| chr12:64620160-64620353 | Rare:33 | ||||
| chr12:64625376-64625636 | Common:1; Rare:42 | ||||
| chr12:64630392-64630716 | Common:2; Rare:48 | ||||
| chr12:64632282-64632454 | Common:2; Rare:36 | ||||
| chr12:64637174-64637409 | Common:1; Rare:35 | ||||
| chr12:64816141-64816164 | Rare:3 | ||||
| chr12:65170083-65170300 | Rare:70; Clinvar:4 | ||||
| chr12:65170529-65170888 | Common:1; Rare:111; Clinvar:4; Clinvar (benign):1 | ||||
| chr12:65170926-65171091 | Rare:36 |