| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:46372698-46372980 | Rare:119 | ||||
| chr12:47079490-47079621 | Common:1; Rare:31 | ||||
| chr12:47705951-47706088 | Rare:61 | ||||
| chr12:48004453-48004678 | Common:2; Rare:40; Clinvar (benign):1 | ||||
| chr12:48105815-48105938 | Rare:28 | ||||
| chr12:48105949-48106194 | Common:2; Rare:81 | ||||
| chr12:48106277-48106385 | Rare:34 | ||||
| chr12:48682196-48682468 | Common:6; Rare:83 | ||||
| chr12:48716664-48717003 | Common:4; Rare:103 | ||||
| chr12:48852086-48852371 | Common:2; Rare:85 | ||||
| chr12:48957367-48957682 | Common:4; Rare:84 | ||||
| chr12:49018741-49018908 | Rare:65 | ||||
| chr12:49069974-49070144 | Common:2; Rare:42 | ||||
| chr12:49110654-49110988 | Rare:73 | ||||
| chr12:49131285-49131606 | Common:2; Rare:130 |