| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:49018741-49018908 | Rare:65 | ||||
| chr12:49188989-49189274 | Rare:79; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:49264749-49265136 | Common:5; Rare:140 | ||||
| chr12:49322954-49323307 | Common:3; Rare:89 | ||||
| chr12:49568110-49568211 | Common:2; Rare:35 | ||||
| chr12:49828411-49828543 | Rare:40 | ||||
| chr12:50085291-50085364 | Common:1; Rare:14 | ||||
| chr12:50283433-50283636 | Rare:59 | ||||
| chr12:50400778-50401004 | Common:1; Rare:70 | ||||
| chr12:50763889-50764113 | Common:2; Rare:67 | ||||
| chr12:51026337-51026561 | Common:4; Rare:94; Clinvar:1; Clinvar (benign):2 | ||||
| chr12:51048119-51048351 | Common:1; Rare:78 | ||||
| chr12:51238648-51238899 | Common:8; Rare:111 | ||||
| chr12:51270276-51270317 | Rare:10 | ||||
| chr12:51270339-51270427 | Common:1; Rare:25 |