| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:88035419-88035589 | Common:1; Rare:49 | ||||
| chr12:88141994-88142396 | Rare:114; Clinvar:4 | ||||
| chr12:88580400-88580556 | Common:2; Rare:54 | ||||
| chr12:89352472-89352747 | Rare:86 | ||||
| chr12:89525283-89525504 | Rare:37 | ||||
| chr12:89525992-89526083 | Rare:35 | ||||
| chr12:92145843-92146148 | Common:1; Rare:89 | ||||
| chr12:92929283-92929521 | Rare:68 | ||||
| chr12:93377773-93377929 | Rare:38 | ||||
| chr12:93441883-93442155 | Common:2; Rare:87 | ||||
| chr12:93571755-93571859 | Common:5; Rare:38 | ||||
| chr12:93677309-93677381 | Rare:16 | ||||
| chr12:94459802-94460041 | Common:3; Rare:68 | ||||
| chr12:95003605-95003804 | Common:3; Rare:85; Clinvar (benign):6 | ||||
| chr12:95217386-95217769 | Common:4; Rare:105 |