| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:178006590-178006791 | Common:1; Rare:6 | ||||
| chr5:178113369-178113676 | Common:3; Rare:99 | ||||
| chr5:178130848-178131033 | Rare:52 | ||||
| chr5:178153749-178154103 | Rare:113; Clinvar:5; Clinvar (benign):1 | ||||
| chr5:178204339-178204534 | Common:3; Rare:68 | ||||
| chr5:178232388-178232531 | Common:6; Rare:83 | ||||
| chr5:178232551-178232896 | Common:4; Rare:113 | ||||
| chr5:178859747-178860086 | Common:4; Rare:97 | ||||
| chr5:178895812-178895937 | Rare:49 | ||||
| chr5:179023641-179023867 | Common:3; Rare:68 | ||||
| chr5:179550450-179550561 | Common:4; Rare:32 | ||||
| chr5:179550808-179550858 | Rare:18 | ||||
| chr5:179559504-179559814 | Common:1; Rare:97 | ||||
| chr5:179623564-179623822 | Common:1; Rare:100 | ||||
| chr5:179698575-179699099 | Common:4; Rare:186 |