| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:57750671-57750920 | Common:1; Rare:56; Clinvar:5; Clinvar (benign):7 | ||||
| chr12:57936162-57936214 | Common:1; Rare:18 | ||||
| chr12:64737085-64737336 | Rare:51; Clinvar:1 | ||||
| chr12:67718665-67718694 | Rare:7 | ||||
| chr12:72432343-72432516 | Common:1; Rare:37 | ||||
| chr12:92466571-92466835 | Common:2; Rare:44 | ||||
| chr12:93314603-93314955 | Common:1; Rare:77 | ||||
| chr12:93737796-93738092 | Common:2; Rare:51 | ||||
| chr12:98503848-98504010 | Common:2; Rare:45 | ||||
| chr12:101717525-101717734 | Common:3; Rare:25 | ||||
| chr12:101748438-101748665 | Rare:42 | ||||
| chr12:101749719-101749748 | Rare:1 | ||||
| chr12:101796700-101796822 | Common:1; Rare:35; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr12:103946644-103946936 | Rare:74 | ||||
| chr12:104457692-104457730 | Rare:7 |