| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:31324101-31324457 | Common:1; Rare:76 | ||||
| chr12:31728995-31729280 | Common:1; Rare:89 | ||||
| chr12:31959258-31959488 | Common:2; Rare:75 | ||||
| chr12:32107542-32107544 | |||||
| chr12:32501999-32502240 | Common:2; Rare:51; Clinvar:3; Clinvar (benign):2 | ||||
| chr12:32679080-32679366 | Common:2; Rare:117; Clinvar:1; Clinvar (benign):4 | ||||
| chr12:32755871-32755991 | Rare:45 | ||||
| chr12:38905491-38905798 | Common:5; Rare:87 | ||||
| chr12:38905987-38906078 | Rare:18 | ||||
| chr12:38906697-38906878 | Common:1; Rare:41 | ||||
| chr12:40692317-40692505 | Common:1; Rare:68 | ||||
| chr12:42325922-42326211 | Common:1; Rare:89 | ||||
| chr12:43758745-43759016 | Common:2; Rare:76; Clinvar:2 | ||||
| chr12:43806090-43806434 | Common:4; Rare:129 | ||||
| chr12:43806605-43806653 | Rare:10 |