| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:172711058-172711387 | Common:1; Rare:79 | ||||
| chr3:172750397-172750789 | Common:4; Rare:88 | ||||
| chr3:174440819-174440987 | Common:2; Rare:50 | ||||
| chr3:179071553-179071908 | Rare:101 | ||||
| chr3:179147938-179148142 | Common:2; Rare:51 | ||||
| chr3:179562670-179563003 | Rare:108 | ||||
| chr3:179604614-179604932 | Common:3; Rare:124 | ||||
| chr3:180601971-180602241 | Common:1; Rare:85 | ||||
| chr3:180989629-180989797 | Rare:74; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:183099444-183099749 | Common:2; Rare:100; Clinvar:3; Clinvar (benign):5 | ||||
| chr3:183635473-183635687 | Common:3; Rare:70 | ||||
| chr3:183884828-183884981 | Rare:60 | ||||
| chr3:184017876-184018092 | Common:1; Rare:68 | ||||
| chr3:184135221-184135395 | Common:2; Rare:53; Clinvar:5 | ||||
| chr3:184185856-184186229 | Common:5; Rare:144 |