| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:25386210-25386402 | Common:1; Rare:72 | ||||
| chr12:29135061-29135233 | Common:4; Rare:38 | ||||
| chr12:29749703-29749868 | Common:1; Rare:27 | ||||
| chr12:31073140-31073263 | Rare:27 | ||||
| chr12:31278853-31279019 | Common:3; Rare:29 | ||||
| chr12:31369077-31369351 | Common:1; Rare:46 | ||||
| chr12:31370967-31371127 | Rare:26 | ||||
| chr12:32377432-32377657 | Common:2; Rare:57 | ||||
| chr12:32585888-32585995 | Rare:17 | ||||
| chr12:32727171-32727459 | Rare:50 | ||||
| chr12:32741272-32741344 | Common:3; Rare:16 | ||||
| chr12:32743135-32743534 | Common:4; Rare:110; Clinvar (benign):4 | ||||
| chr12:33588260-33588444 | Rare:36 | ||||
| chr12:42313730-42313931 | Common:1; Rare:62 | ||||
| chr12:44519842-44520085 | Common:3; Rare:61 |