| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:104986763-104986804 | Rare:9 | ||||
| chr12:105084530-105084780 | Common:2; Rare:69 | ||||
| chr12:105107350-105107448 | Common:1; Rare:23 | ||||
| chr12:105107466-105107865 | Common:2; Rare:149; Clinvar:1 | ||||
| chr12:105108161-105108244 | Rare:22 | ||||
| chr12:105236068-105236354 | Common:3; Rare:134 | ||||
| chr12:105330239-105330352 | Rare:23 | ||||
| chr12:105330402-105330870 | Common:4; Rare:141 | ||||
| chr12:106247914-106248022 | Rare:33 | ||||
| chr12:106301838-106301906 | Rare:15 | ||||
| chr12:106301908-106301965 | Rare:9 | ||||
| chr12:106302247-106302653 | Common:13; Rare:129 | ||||
| chr12:106357521-106357857 | Common:3; Rare:73; Clinvar:4; Clinvar (benign):1 | ||||
| chr12:106357914-106358331 | Common:5; Rare:144 | ||||
| chr12:106358516-106358581 | Common:1; Rare:9 |