| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:48119186-48119396 | Common:2; Rare:41; Clinvar:4; Clinvar (benign):2 | ||||
| chr12:48350787-48350963 | Rare:64 | ||||
| chr12:49018739-49018858 | Rare:53 | ||||
| chr12:49131299-49131592 | Rare:118 | ||||
| chr12:49188487-49188583 | Common:1; Rare:14 | ||||
| chr12:49188981-49189206 | Rare:61; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:49264781-49265096 | Common:4; Rare:114 | ||||
| chr12:49367220-49367524 | Common:1; Rare:84 | ||||
| chr12:49568098-49568216 | Common:2; Rare:41 | ||||
| chr12:49828368-49828579 | Common:1; Rare:81 | ||||
| chr12:50085064-50085380 | Common:1; Rare:85 | ||||
| chr12:50103881-50104034 | Rare:34 | ||||
| chr12:50283452-50283652 | Common:1; Rare:62 | ||||
| chr12:50763769-50764297 | Common:2; Rare:141 | ||||
| chr12:50924514-50924740 | Common:3; Rare:74 |