| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:8942447-8942618 | Rare:43 | ||||
| chr12:8949945-8950099 | Common:1; Rare:45 | ||||
| chr12:9115817-9115998 | Common:3; Rare:45 | ||||
| chr12:9607435-9607607 | Common:1; Rare:42 | ||||
| chr12:10505839-10505897 | Rare:27 | ||||
| chr12:10613504-10613643 | Rare:59 | ||||
| chr12:10722881-10723022 | Common:3; Rare:50 | ||||
| chr12:11171163-11171243 | Rare:34 | ||||
| chr12:11171551-11171638 | Common:1; Rare:29 | ||||
| chr12:12356981-12357324 | Common:6; Rare:149 | ||||
| chr12:12611702-12612019 | Common:2; Rare:101 | ||||
| chr12:12717234-12717552 | Common:1; Rare:100; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:12717581-12717907 | Common:1; Rare:109; Clinvar:9; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr12:12891291-12891663 | Common:1; Rare:70 | ||||
| chr12:13000050-13000468 | Common:2; Rare:132 |