| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:53487326-53487517 | Common:1; Rare:52 | ||||
| chr12:53499436-53499727 | Rare:63 | ||||
| chr12:53501118-53501456 | Rare:87 | ||||
| chr12:53501543-53501715 | Rare:38 | ||||
| chr12:53676027-53676389 | Common:3; Rare:173 | ||||
| chr12:53715932-53716361 | Common:3; Rare:103 | ||||
| chr12:54284007-54284318 | Common:2; Rare:87; Clinvar (benign):1 | ||||
| chr12:54419019-54419128 | Rare:39 | ||||
| chr12:54419171-54419593 | Common:1; Rare:101 | ||||
| chr12:55716003-55716193 | Common:1; Rare:90 | ||||
| chr12:55716723-55717005 | Rare:69 | ||||
| chr12:55720177-55720541 | Common:4; Rare:56; Clinvar:3; Clinvar (benign):1 | ||||
| chr12:55725809-55726000 | Rare:34 | ||||
| chr12:55726020-55726322 | Common:1; Rare:87 | ||||
| chr12:55726690-55726980 | Common:2; Rare:95 |