| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:130314395-130314509 | Common:1; Rare:37 | ||||
| chr11:134253306-134253586 | Common:2; Rare:90; Clinvar (benign):1 | ||||
| chr12:389236-389398 | Common:1; Rare:63 | ||||
| chr12:401440-401644 | Rare:56 | ||||
| chr12:643624-643666 | Rare:6 | ||||
| chr12:2004439-2004669 | Common:2; Rare:67 | ||||
| chr12:2877039-2877254 | Rare:65 | ||||
| chr12:3873355-3873514 | Common:1; Rare:36 | ||||
| chr12:4538436-4538795 | Rare:74 | ||||
| chr12:4648966-4649154 | Common:2; Rare:63; Clinvar (benign):1 | ||||
| chr12:6124528-6124877 | Rare:44; Clinvar:1 | ||||
| chr12:6200031-6200416 | Common:3; Rare:104 | ||||
| chr12:6375364-6375654 | Common:3; Rare:75; Clinvar:1; Clinvar (benign):6 | ||||
| chr12:6452078-6452120 | Common:1; Rare:11 | ||||
| chr12:6493240-6493386 | Common:5; Rare:41 |