| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:9647978-9648178 | Common:4; Rare:66 | ||||
| chr12:11556288-11556530 | Common:1; Rare:49 | ||||
| chr12:11701612-11701698 | Rare:13 | ||||
| chr12:12110738-12110986 | Rare:48 | ||||
| chr12:15688454-15688534 | Common:1; Rare:12 | ||||
| chr12:25386193-25386383 | Common:1; Rare:75 | ||||
| chr12:32742339-32742682 | Common:1; Rare:62; Clinvar (benign):1 | ||||
| chr12:45727448-45727839 | Rare:159 | ||||
| chr12:47789260-47789423 | Rare:41 | ||||
| chr12:52032950-52033260 | Common:1; Rare:94 | ||||
| chr12:53038244-53038406 | Common:3; Rare:39 | ||||
| chr12:53100757-53101156 | Common:3; Rare:137 | ||||
| chr12:54081319-54081532 | Common:2; Rare:43 | ||||
| chr12:54081866-54081993 | Common:1; Rare:25 | ||||
| chr12:54125993-54126244 | Common:1; Rare:53 |