| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:105107540-105107891 | Common:2; Rare:141; Clinvar:1 | ||||
| chr12:105108131-105108254 | Rare:33 | ||||
| chr12:105235721-105236380 | Common:4; Rare:238 | ||||
| chr12:105330478-105330904 | Common:4; Rare:131 | ||||
| chr12:106139052-106139566 | Common:4; Rare:150 | ||||
| chr12:106247508-106247591 | Common:1; Rare:31 | ||||
| chr12:106247871-106248372 | Common:2; Rare:139 | ||||
| chr12:106301832-106301976 | Rare:27 | ||||
| chr12:106302481-106302855 | Common:6; Rare:95 | ||||
| chr12:106302888-106302993 | Common:3; Rare:17 | ||||
| chr12:106303288-106303485 | Common:1; Rare:46 | ||||
| chr12:106357686-106357837 | Common:3; Rare:35; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:106357870-106358193 | Common:4; Rare:133; Clinvar:1 | ||||
| chr12:106358217-106358300 | Common:1; Rare:15 | ||||
| chr12:106358302-106358405 | Common:1; Rare:22 |