| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:31326111-31326292 | Common:3; Rare:65 | ||||
| chr12:31729010-31729213 | Rare:60 | ||||
| chr12:31958916-31959161 | Common:2; Rare:54 | ||||
| chr12:31959262-31959488 | Common:2; Rare:73 | ||||
| chr12:32106675-32106875 | Common:3; Rare:58 | ||||
| chr12:32679086-32679358 | Common:2; Rare:108; Clinvar:1; Clinvar (benign):4 | ||||
| chr12:32896764-32896996 | Common:3; Rare:78; Clinvar:4; Clinvar (benign):2 | ||||
| chr12:38905580-38905789 | Common:5; Rare:57 | ||||
| chr12:39443304-39443446 | Rare:47; Clinvar:3; Clinvar (benign):1 | ||||
| chr12:39619732-39619941 | Common:1; Rare:35 | ||||
| chr12:40692290-40692585 | Common:1; Rare:90 | ||||
| chr12:42326006-42326207 | Common:1; Rare:64 | ||||
| chr12:43758745-43759011 | Common:2; Rare:74; Clinvar:2 | ||||
| chr12:43806221-43806356 | Common:1; Rare:48 | ||||
| chr12:44875266-44875446 | Rare:53 |