| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:1555121-1555317 | Rare:36 | ||||
| chr12:1594696-1595053 | Common:4; Rare:104 | ||||
| chr12:1601338-1601640 | Common:1; Rare:50 | ||||
| chr12:1601647-1602058 | Common:3; Rare:81 | ||||
| chr12:1605287-1605461 | Rare:39 | ||||
| chr12:1605726-1605818 | Common:2; Rare:16 | ||||
| chr12:1606051-1606481 | Common:2; Rare:90 | ||||
| chr12:1661938-1662285 | Common:3; Rare:100 | ||||
| chr12:1804620-1804785 | Common:1; Rare:41 | ||||
| chr12:2691026-2691325 | Common:1; Rare:93; Clinvar:11; Clinvar (benign):5 | ||||
| chr12:2691810-2691851 | Rare:11 | ||||
| chr12:3704911-3704981 | Rare:12 | ||||
| chr12:4107470-4107628 | Common:1; Rare:29 | ||||
| chr12:4107738-4107780 | Rare:10 | ||||
| chr12:4115110-4115254 | Common:2; Rare:18 |