| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:38906179-38906629 | Common:2; Rare:95 | ||||
| chr12:39442926-39443099 | Common:1; Rare:44; Clinvar:1; Clinvar (benign):2 | ||||
| chr12:39443296-39443446 | Rare:49; Clinvar:4; Clinvar (benign):1 | ||||
| chr12:39619804-39619912 | Common:1; Rare:21 | ||||
| chr12:39626126-39626250 | Rare:38 | ||||
| chr12:40105581-40105644 | Rare:23 | ||||
| chr12:40224704-40225026 | Common:5; Rare:73; Clinvar (benign):1 | ||||
| chr12:40692317-40692514 | Common:1; Rare:73 | ||||
| chr12:41188780-41189012 | Common:4; Rare:94 | ||||
| chr12:42238153-42238496 | Common:4; Rare:113 | ||||
| chr12:42325922-42326255 | Common:2; Rare:102 | ||||
| chr12:42331670-42331833 | Common:2; Rare:30 | ||||
| chr12:42483949-42484093 | Common:1; Rare:15 | ||||
| chr12:43758728-43759020 | Common:2; Rare:85; Clinvar:2 | ||||
| chr12:43806221-43806393 | Common:2; Rare:56 |