| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:50025359-50025703 | Common:2; Rare:95 | ||||
| chr12:50085066-50085384 | Common:1; Rare:88 | ||||
| chr12:50085451-50085537 | Rare:16 | ||||
| chr12:50112032-50112325 | Common:2; Rare:64; Clinvar (benign):1 | ||||
| chr12:50167290-50167450 | Common:2; Rare:58 | ||||
| chr12:50202415-50202485 | Rare:18 | ||||
| chr12:50283461-50283669 | Common:3; Rare:64 | ||||
| chr12:50400754-50401202 | Common:1; Rare:133 | ||||
| chr12:50401340-50401503 | Common:1; Rare:34 | ||||
| chr12:50763203-50763592 | Common:6; Rare:69 | ||||
| chr12:50763931-50764359 | Common:1; Rare:114 | ||||
| chr12:51026321-51026517 | Common:3; Rare:86; Clinvar:1; Clinvar (benign):2 | ||||
| chr12:51048212-51048377 | Common:1; Rare:80 | ||||
| chr12:51172805-51173247 | Common:2; Rare:94 | ||||
| chr12:51238743-51238990 | Common:1; Rare:105 |