| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:52056226-52056435 | Common:3; Rare:35 | ||||
| chr12:52451632-52451703 | Common:1; Rare:36 | ||||
| chr12:52451836-52452188 | Common:4; Rare:127 | ||||
| chr12:52473036-52473362 | Common:7; Rare:80 | ||||
| chr12:52473368-52473546 | Common:3; Rare:54 | ||||
| chr12:52489912-52490236 | Common:5; Rare:90 | ||||
| chr12:52491209-52491884 | Common:12; Rare:221 | ||||
| chr12:52515950-52516158 | Common:1; Rare:35 | ||||
| chr12:52517095-52517778 | Common:3; Rare:173; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr12:52518451-52518717 | Common:3; Rare:48 | ||||
| chr12:52519605-52520407 | Common:8; Rare:262; Clinvar:12; Clinvar (benign):12; Clinvar (pathogenic):4 | ||||
| chr12:52520434-52520609 | Rare:35 | ||||
| chr12:52679756-52680053 | Rare:94; Clinvar:4 | ||||
| chr12:52813595-52813833 | Common:5; Rare:96; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr12:52848590-52849043 | Common:8; Rare:154 |