| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:94459802-94460047 | Common:3; Rare:70 | ||||
| chr12:95003605-95003827 | Common:3; Rare:91; Clinvar (benign):6 | ||||
| chr12:95217347-95217769 | Common:6; Rare:112 | ||||
| chr12:95474055-95474255 | Common:2; Rare:94 | ||||
| chr12:95548796-95548903 | Common:2; Rare:40 | ||||
| chr12:95858815-95859033 | Common:2; Rare:60 | ||||
| chr12:96400531-96400822 | Common:1; Rare:101 | ||||
| chr12:96907139-96907293 | Common:1; Rare:53 | ||||
| chr12:98515475-98515767 | Rare:92; Clinvar:2 | ||||
| chr12:98593484-98593801 | Common:2; Rare:102; Clinvar:4; Clinvar (benign):4 | ||||
| chr12:98644712-98645302 | Common:7; Rare:172 | ||||
| chr12:100200707-100200834 | Rare:39 | ||||
| chr12:100267060-100267299 | Common:1; Rare:107 | ||||
| chr12:100573554-100573740 | Rare:65 | ||||
| chr12:101407693-101408035 | Common:3; Rare:78 |