| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:12891306-12891617 | Common:1; Rare:63 | ||||
| chr12:13000169-13000481 | Common:2; Rare:95 | ||||
| chr12:13044296-13044392 | Rare:19 | ||||
| chr12:14365466-14365714 | Common:1; Rare:82 | ||||
| chr12:14774184-14774517 | Common:3; Rare:89 | ||||
| chr12:14803439-14803715 | Common:1; Rare:72 | ||||
| chr12:15882261-15882621 | Common:1; Rare:114 | ||||
| chr12:16347497-16347743 | Common:4; Rare:46 | ||||
| chr12:19129425-19129772 | Common:3; Rare:141 | ||||
| chr12:21437592-21437731 | Common:5; Rare:58 | ||||
| chr12:21501556-21501900 | Common:4; Rare:88 | ||||
| chr12:21657758-21657980 | Common:4; Rare:78; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:22544470-22544681 | Common:2; Rare:47 | ||||
| chr12:22624870-22625275 | Common:2; Rare:159 | ||||
| chr12:24948986-24949162 | Common:1; Rare:43 |