| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:171387491-171388006 | Common:1; Rare:240; Clinvar:1 | ||||
| chr5:172959371-172959490 | Common:1; Rare:42 | ||||
| chr5:172983677-172983854 | Common:1; Rare:67 | ||||
| chr5:173328411-173328586 | Rare:31 | ||||
| chr5:173917911-173918201 | Common:1; Rare:64 | ||||
| chr5:176388558-176388812 | Common:4; Rare:99 | ||||
| chr5:177022610-177022732 | Rare:45 | ||||
| chr5:177133474-177133877 | Rare:144 | ||||
| chr5:177133997-177134158 | Common:1; Rare:47 | ||||
| chr5:177303691-177304008 | Common:3; Rare:126 | ||||
| chr5:177351643-177351720 | Rare:20 | ||||
| chr5:177497548-177497819 | Common:1; Rare:97 | ||||
| chr5:177516932-177517019 | Rare:38; Clinvar (pathogenic):1 | ||||
| chr5:177592051-177592207 | Common:1; Rare:55 | ||||
| chr5:178153825-178154083 | Rare:79; Clinvar:4; Clinvar (benign):1 |