| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:31728683-31729513 | Common:4; Rare:211 | ||||
| chr12:31959153-31959694 | Common:4; Rare:163 | ||||
| chr12:31959856-31959893 | Rare:7 | ||||
| chr12:31960006-31960113 | Rare:25 | ||||
| chr12:32106512-32107087 | Common:6; Rare:156 | ||||
| chr12:32399408-32399581 | Common:2; Rare:37 | ||||
| chr12:32679048-32679350 | Common:2; Rare:117; Clinvar:1; Clinvar (benign):3 | ||||
| chr12:32679638-32679818 | Rare:41 | ||||
| chr12:32755138-32755561 | Common:1; Rare:147; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr12:32755764-32756100 | Common:1; Rare:116; Clinvar (benign):1 | ||||
| chr12:34022127-34022689 | Common:4; Rare:147 | ||||
| chr12:38316453-38316872 | Common:7; Rare:103 | ||||
| chr12:38904800-38905357 | Common:3; Rare:116 | ||||
| chr12:38905390-38905426 | Rare:12 | ||||
| chr12:38905502-38906072 | Common:7; Rare:154 |