| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:8949951-8950099 | Common:1; Rare:43 | ||||
| chr12:9101145-9101274 | Rare:29 | ||||
| chr12:9115845-9116157 | Common:3; Rare:61 | ||||
| chr12:9869352-9869559 | Common:2; Rare:34 | ||||
| chr12:10213510-10213861 | Common:2; Rare:77 | ||||
| chr12:10722878-10723022 | Common:3; Rare:52 | ||||
| chr12:10723134-10723613 | Common:6; Rare:151 | ||||
| chr12:11171158-11171232 | Rare:31 | ||||
| chr12:11171507-11171648 | Common:2; Rare:40 | ||||
| chr12:12356986-12357125 | Common:1; Rare:74 | ||||
| chr12:12611654-12612113 | Common:2; Rare:132 | ||||
| chr12:12717181-12717496 | Rare:108; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:12717612-12717873 | Common:1; Rare:82; Clinvar:7; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr12:12725253-12725570 | Common:3; Rare:77 | ||||
| chr12:12725634-12725942 | Common:4; Rare:72 |