| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:48815245-48815700 | Common:6; Rare:392 | ||||
| chr12:48818350-48818888 | Common:1; Rare:254 | ||||
| chr12:48851565-48851965 | Common:2; Rare:68 | ||||
| chr12:48852000-48852610 | Common:23; Rare:790 | ||||
| chr12:48852523-48853376 | Common:7; Rare:334 | ||||
| chr12:48853284-48853506 | Rare:56 | ||||
| chr12:48865485-48866026 | Common:1; Rare:237 | ||||
| chr12:48956360-48957288 | Common:19; Rare:416 | ||||
| chr12:48957210-48957767 | Common:16; Rare:407 | ||||
| chr12:48971190-48972000 | Common:35; Rare:298 | ||||
| chr12:48999242-49000139 | Common:5; Rare:260 | ||||
| chr12:49017058-49018240 | Common:2; Rare:243 | ||||
| chr12:49018639-49018992 | Common:6; Rare:597; Clinvar (benign):1 | ||||
| chr12:49019041-49020113 | Common:5; Rare:258; Clinvar:6; Clinvar (benign):12 | ||||
| chr12:49059362-49059762 | Rare:88 |