| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:52051152-52051458 | Common:1; Rare:100 | ||||
| chr12:52185597-52185833 | Rare:56 | ||||
| chr12:52191606-52191687 | Rare:27 | ||||
| chr12:52191697-52191750 | Rare:17 | ||||
| chr12:52519742-52520453 | Common:7; Rare:244; Clinvar:12; Clinvar (benign):12; Clinvar (pathogenic):4 | ||||
| chr12:52651556-52652258 | Common:9; Rare:284; Clinvar:2; Clinvar (benign):10 | ||||
| chr12:52679708-52680072 | Common:1; Rare:119; Clinvar:4 | ||||
| chr12:52848087-52848363 | Rare:103 | ||||
| chr12:52848689-52848879 | Common:4; Rare:77 | ||||
| chr12:52848902-52849149 | Common:1; Rare:61 | ||||
| chr12:53049878-53050085 | Rare:51 | ||||
| chr12:53180638-53180730 | Common:1; Rare:30 | ||||
| chr12:53231871-53232024 | Rare:41 | ||||
| chr12:53232106-53232432 | Common:2; Rare:68 | ||||
| chr12:53232764-53232934 | Rare:26 |