| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:177263814-177264177 | Common:2; Rare:99 | ||||
| chr2:177264537-177264887 | Common:2; Rare:101 | ||||
| chr2:177264932-177265105 | Common:1; Rare:34 | ||||
| chr2:177392583-177393090 | Common:4; Rare:167; Clinvar:6; Clinvar (benign):4 | ||||
| chr2:177552755-177553103 | Common:4; Rare:109 | ||||
| chr2:177618658-177618749 | Common:1; Rare:48 | ||||
| chr2:177618948-177619010 | Rare:8 | ||||
| chr2:178108282-178108431 | Common:2; Rare:41 | ||||
| chr2:178112335-178112531 | Common:1; Rare:64 | ||||
| chr2:178450683-178450912 | Common:1; Rare:88 | ||||
| chr2:178451083-178451666 | Common:6; Rare:166; Clinvar:9; Clinvar (benign):3 | ||||
| chr2:178478271-178478699 | Common:1; Rare:135 | ||||
| chr2:178479983-178480376 | Common:1; Rare:104 | ||||
| chr2:178480717-178480829 | Common:1; Rare:36 | ||||
| chr2:179049975-179050032 | Rare:11 |