| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:14365490-14365748 | Common:1; Rare:85 | ||||
| chr12:14466526-14466638 | Rare:34 | ||||
| chr12:14803351-14803715 | Common:3; Rare:101 | ||||
| chr12:14948863-14949044 | Common:1; Rare:28 | ||||
| chr12:15789156-15789539 | Common:1; Rare:115 | ||||
| chr12:15882308-15882818 | Common:1; Rare:158 | ||||
| chr12:15900821-15901024 | Rare:49 | ||||
| chr12:16347240-16347879 | Common:6; Rare:111 | ||||
| chr12:19439216-19439743 | Common:4; Rare:184 | ||||
| chr12:21437611-21437809 | Common:5; Rare:89 | ||||
| chr12:21501532-21501949 | Common:5; Rare:118 | ||||
| chr12:21657746-21658040 | Common:4; Rare:95; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:21941217-21941320 | Rare:19 | ||||
| chr12:22046382-22046551 | Rare:55 | ||||
| chr12:22458630-22458851 | Common:1; Rare:49 |