| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:48119141-48119371 | Common:2; Rare:46; Clinvar:4; Clinvar (benign):2 | ||||
| chr12:48119681-48119709 | Rare:3 | ||||
| chr12:48157060-48157144 | Rare:18 | ||||
| chr12:48157422-48157806 | Common:5; Rare:96 | ||||
| chr12:48350873-48351183 | Common:7; Rare:106 | ||||
| chr12:48681260-48681582 | Common:2; Rare:81 | ||||
| chr12:48681781-48681802 | Rare:9 | ||||
| chr12:48682171-48682541 | Common:6; Rare:122 | ||||
| chr12:48716636-48717190 | Common:6; Rare:172 | ||||
| chr12:48717376-48717595 | Rare:40 | ||||
| chr12:48788845-48788908 | Rare:11 | ||||
| chr12:48789071-48789140 | Rare:11 | ||||
| chr12:48814659-48814958 | Rare:53 | ||||
| chr12:48815159-48815306 | Rare:38 | ||||
| chr12:48815391-48815591 | Common:1; Rare:49 |