| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6867132-6867569 | Common:2; Rare:144; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:6868023-6868185 | Common:5; Rare:67 | ||||
| chr12:6873279-6873669 | Common:4; Rare:113 | ||||
| chr12:6904732-6905196 | Common:2; Rare:107 | ||||
| chr12:6914355-6914659 | Common:2; Rare:75 | ||||
| chr12:6927881-6928381 | Common:3; Rare:113 | ||||
| chr12:6943531-6944172 | Common:18; Rare:498; Clinvar:6; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:6970616-6970977 | Common:4; Rare:116; Clinvar (benign):1 | ||||
| chr12:7018360-7018707 | Common:2; Rare:103 | ||||
| chr12:7130221-7130472 | Common:5; Rare:63 | ||||
| chr12:7189551-7189733 | Rare:67; Clinvar:4 | ||||
| chr12:8032583-8032802 | Common:3; Rare:74 | ||||
| chr12:8082671-8082807 | Common:7; Rare:39 | ||||
| chr12:8697389-8697428 | Rare:12 | ||||
| chr12:8697884-8698275 | Common:5; Rare:140 |