| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:62259804-62260520 | Common:3; Rare:495 | ||||
| chr12:62466564-62466945 | Common:1; Rare:264 | ||||
| chr12:62466951-62467190 | Common:2; Rare:67 | ||||
| chr12:62467110-62467510 | Common:2; Rare:164 | ||||
| chr12:62933217-62934040 | Common:8; Rare:257 | ||||
| chr12:62934810-62935423 | Common:4; Rare:296 | ||||
| chr12:63779656-63779961 | Common:5; Rare:162; Clinvar (benign):2 | ||||
| chr12:63780029-63780287 | Rare:197; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):5 | ||||
| chr12:63843597-63844310 | Common:14; Rare:302 | ||||
| chr12:63844301-63844881 | Common:5; Rare:353 | ||||
| chr12:64221669-64222040 | Rare:76 | ||||
| chr12:64222130-64222392 | Rare:196 | ||||
| chr12:64222495-64222650 | Rare:42 | ||||
| chr12:64404117-64404745 | Common:17; Rare:532 | ||||
| chr12:64404949-64405167 | Rare:72 |