| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:52451660-52452233 | Common:7; Rare:197; Clinvar (benign):1 | ||||
| chr12:52473187-52473380 | Common:3; Rare:56 | ||||
| chr12:52473474-52474064 | Common:11; Rare:204 | ||||
| chr12:52492642-52493397 | Common:5; Rare:237; Clinvar:2; Clinvar (pathogenic):3 | ||||
| chr12:52515791-52515861 | Rare:21; Clinvar (pathogenic):1 | ||||
| chr12:52517101-52517566 | Common:2; Rare:113; Clinvar (benign):2 | ||||
| chr12:52517812-52518008 | Rare:52; Clinvar:1 | ||||
| chr12:52518451-52518742 | Common:3; Rare:52 | ||||
| chr12:52519410-52519451 | Rare:6 | ||||
| chr12:52519733-52520481 | Common:7; Rare:253; Clinvar:12; Clinvar (benign):12; Clinvar (pathogenic):4 | ||||
| chr12:52813590-52813855 | Common:7; Rare:108; Clinvar:4; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr12:52813858-52814485 | Common:1; Rare:186; Clinvar:3; Clinvar (benign):2 | ||||
| chr12:52848277-52848706 | Common:5; Rare:106 | ||||
| chr12:52848709-52849310 | Common:7; Rare:168 | ||||
| chr12:52948787-52949167 | Common:2; Rare:94; Clinvar:1 |