| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:175181756-175181811 | Rare:14 | ||||
| chr2:176002220-176002414 | Common:3; Rare:85 | ||||
| chr2:176129586-176129730 | Rare:84 | ||||
| chr2:176269363-176269516 | Common:1; Rare:60 | ||||
| chr2:177212422-177212836 | Common:4; Rare:165 | ||||
| chr2:177213056-177213293 | Rare:107 | ||||
| chr2:177263402-177263602 | Rare:46 | ||||
| chr2:177263802-177263953 | Common:1; Rare:39 | ||||
| chr2:177264533-177264845 | Common:2; Rare:90 | ||||
| chr2:177265034-177265197 | Rare:38 | ||||
| chr2:177314846-177315016 | Rare:17 | ||||
| chr2:177392657-177393090 | Common:3; Rare:148; Clinvar:6; Clinvar (benign):4 | ||||
| chr2:177552761-177552838 | Common:1; Rare:29 | ||||
| chr2:178450689-178450897 | Common:1; Rare:70 | ||||
| chr2:178451083-178451615 | Common:6; Rare:146; Clinvar:9; Clinvar (benign):3 |