| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:49828362-49828683 | Common:1; Rare:104 | ||||
| chr12:49992074-49992282 | Common:2; Rare:54 | ||||
| chr12:50085052-50085368 | Common:1; Rare:84 | ||||
| chr12:50085483-50085544 | Rare:9 | ||||
| chr12:50098736-50099104 | Common:1; Rare:83 | ||||
| chr12:50112129-50112325 | Common:1; Rare:46; Clinvar (benign):1 | ||||
| chr12:50143170-50143352 | Common:1; Rare:42 | ||||
| chr12:50166786-50166821 | Rare:6 | ||||
| chr12:50166832-50166881 | Rare:11 | ||||
| chr12:50196544-50196573 | Rare:5 | ||||
| chr12:50201934-50202043 | Rare:21 | ||||
| chr12:50202338-50202751 | Common:1; Rare:69 | ||||
| chr12:50222500-50222778 | Common:1; Rare:56 | ||||
| chr12:50283430-50283671 | Common:3; Rare:72 | ||||
| chr12:50400781-50401016 | Common:1; Rare:77 |