| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:63668285-63668574 | Common:1; Rare:90 | ||||
| chr12:63779667-63779956 | Common:3; Rare:103; Clinvar (benign):1 | ||||
| chr12:63780068-63780169 | Rare:48; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr12:63843864-63844253 | Common:4; Rare:85 | ||||
| chr12:63844530-63844870 | Common:1; Rare:94 | ||||
| chr12:64221756-64221906 | Rare:34 | ||||
| chr12:64222259-64222424 | Common:1; Rare:46 | ||||
| chr12:64404122-64404700 | Common:7; Rare:192 | ||||
| chr12:64404890-64405160 | Rare:119 | ||||
| chr12:64451983-64452184 | Common:1; Rare:77 | ||||
| chr12:64610258-64610531 | Common:4; Rare:93 | ||||
| chr12:64759354-64759707 | Common:3; Rare:99; Clinvar:3 | ||||
| chr12:65169409-65169664 | Common:1; Rare:95; Clinvar:2 | ||||
| chr12:65278596-65278739 | Rare:39 | ||||
| chr12:65279015-65279146 | Rare:30 |