| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:9933546-9933898 | Common:3; Rare:139; Clinvar:2 | ||||
| chr3:9952297-9952478 | Common:1; Rare:37 | ||||
| chr3:10011056-10011279 | Common:1; Rare:64 | ||||
| chr3:10026299-10026498 | Rare:62 | ||||
| chr3:10108207-10108421 | Common:4; Rare:48 | ||||
| chr3:10115473-10115800 | Common:4; Rare:110 | ||||
| chr3:10141654-10142009 | Common:2; Rare:164; Clinvar:39; Clinvar (benign):34 | ||||
| chr3:10142132-10142144 | Rare:4; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:10321011-10321232 | Common:2; Rare:97 | ||||
| chr3:11272306-11272437 | Common:1; Rare:30 | ||||
| chr3:11308774-11308897 | Rare:22 | ||||
| chr3:11582314-11582419 | Rare:30 | ||||
| chr3:11610353-11610627 | Common:2; Rare:61 | ||||
| chr3:11719419-11719620 | Rare:64 | ||||
| chr3:11846843-11846926 | Rare:23 |