| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:11170861-11171250 | Common:5; Rare:105 | ||||
| chr12:11171551-11171648 | Common:2; Rare:31 | ||||
| chr12:12356980-12357187 | Common:4; Rare:109 | ||||
| chr12:12611627-12612113 | Common:2; Rare:139 | ||||
| chr12:12717828-12717883 | Rare:25; Clinvar:8; Clinvar (benign):3 | ||||
| chr12:12725649-12725951 | Common:3; Rare:68 | ||||
| chr12:12891364-12891567 | Common:1; Rare:36 | ||||
| chr12:13000190-13000441 | Common:1; Rare:84 | ||||
| chr12:14365544-14365743 | Common:1; Rare:76 | ||||
| chr12:14567664-14567976 | Common:2; Rare:72 | ||||
| chr12:14771104-14771264 | Rare:63 | ||||
| chr12:14774184-14774662 | Common:3; Rare:155 | ||||
| chr12:14803414-14803699 | Common:2; Rare:77 | ||||
| chr12:14961546-14961726 | Common:2; Rare:46 | ||||
| chr12:15221298-15221586 | Common:1; Rare:89 |