| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:57755660-57755718 | Common:1; Rare:16 | ||||
| chr12:57765183-57765609 | Common:2; Rare:168; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr12:57765615-57765807 | Common:1; Rare:42 | ||||
| chr12:57766191-57766639 | Common:1; Rare:102 | ||||
| chr12:57771402-57771514 | Rare:17 | ||||
| chr12:57771763-57771944 | Rare:39 | ||||
| chr12:57772005-57772372 | Common:1; Rare:110 | ||||
| chr12:57772409-57772796 | Common:5; Rare:86 | ||||
| chr12:57772802-57772913 | Common:1; Rare:26 | ||||
| chr12:57772929-57773031 | Rare:39 | ||||
| chr12:57773093-57773196 | Rare:26 | ||||
| chr12:57845090-57845247 | Common:1; Rare:30 | ||||
| chr12:57845346-57845774 | Common:3; Rare:110 | ||||
| chr12:57845781-57845909 | Common:1; Rare:25 | ||||
| chr12:57846382-57846786 | Common:1; Rare:137 |