| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:30754953-30755171 | Common:3; Rare:77 | ||||
| chr12:31073753-31073907 | Common:8; Rare:57 | ||||
| chr12:31074089-31074265 | Common:1; Rare:36 | ||||
| chr12:31326047-31326439 | Common:4; Rare:131 | ||||
| chr12:31729012-31729267 | Rare:74 | ||||
| chr12:31959293-31959458 | Common:2; Rare:52 | ||||
| chr12:32679050-32679326 | Common:1; Rare:102; Clinvar (benign):1 | ||||
| chr12:32755853-32756036 | Common:1; Rare:66 | ||||
| chr12:42238193-42238462 | Rare:94 | ||||
| chr12:42326008-42326210 | Common:1; Rare:66 | ||||
| chr12:43758749-43759007 | Common:2; Rare:72; Clinvar:2 | ||||
| chr12:43806236-43806418 | Common:2; Rare:62 | ||||
| chr12:45215987-45216240 | Common:1; Rare:74 | ||||
| chr12:45990437-45990944 | Common:2; Rare:165 | ||||
| chr12:46268608-46268857 | Common:1; Rare:68 |