| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:118135983-118136344 | Common:2; Rare:100 | ||||
| chr12:118138968-118139097 | Common:1; Rare:31 | ||||
| chr12:118372617-118373189 | Common:3; Rare:139 | ||||
| chr12:119178573-119178976 | Common:2; Rare:73; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:119668102-119668204 | Common:1; Rare:21 | ||||
| chr12:120116603-120116933 | Common:5; Rare:86 | ||||
| chr12:120197319-120197569 | Common:2; Rare:72 | ||||
| chr12:120200316-120200424 | Rare:27 | ||||
| chr12:120200832-120201372 | Common:3; Rare:166 | ||||
| chr12:120438012-120438126 | Rare:35; Clinvar (benign):1 | ||||
| chr12:120446226-120446479 | Common:1; Rare:91 | ||||
| chr12:120469498-120469889 | Common:5; Rare:133 | ||||
| chr12:120495845-120496215 | Common:7; Rare:127 | ||||
| chr12:120686947-120687209 | Common:2; Rare:89 | ||||
| chr12:120687314-120687528 | Common:1; Rare:53 |