| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:176122503-176122524 | Rare:7 | ||||
| chr5:176133580-176133986 | Common:1; Rare:85 | ||||
| chr5:176397942-176398255 | Common:1; Rare:76 | ||||
| chr5:176541522-176541707 | Common:3; Rare:33 | ||||
| chr5:177434911-177435103 | Common:1; Rare:54 | ||||
| chr5:177440823-177440947 | Common:1; Rare:35 | ||||
| chr5:177468884-177469096 | Rare:56 | ||||
| chr5:177546372-177546650 | Common:1; Rare:48 | ||||
| chr5:177632400-177632422 | Rare:4 | ||||
| chr5:178206576-178206864 | Common:2; Rare:85 | ||||
| chr5:178667980-178668198 | Common:4; Rare:42 | ||||
| chr5:179126626-179126853 | Rare:43 | ||||
| chr5:179169186-179169243 | Rare:6 | ||||
| chr5:179530672-179530829 | Rare:34 | ||||
| chr5:179833454-179833738 | Common:7; Rare:107; Clinvar:4; Clinvar (benign):6 |