| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:175478423-175478609 | Common:1; Rare:66 | ||||
| chr5:175871259-175871696 | Common:3; Rare:140 | ||||
| chr5:175968209-175968380 | Common:2; Rare:34 | ||||
| chr5:176361746-176361906 | Common:1; Rare:45 | ||||
| chr5:176388569-176388822 | Common:4; Rare:103 | ||||
| chr5:176416368-176416652 | Common:1; Rare:83 | ||||
| chr5:176448188-176448402 | Common:1; Rare:76 | ||||
| chr5:176610010-176610212 | Common:1; Rare:83 | ||||
| chr5:177022612-177022746 | Rare:51 | ||||
| chr5:177133438-177133800 | Rare:127 | ||||
| chr5:177303678-177304042 | Common:3; Rare:141 | ||||
| chr5:177351640-177351968 | Rare:82 | ||||
| chr5:177516887-177517100 | Common:2; Rare:81; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr5:177592088-177592216 | Common:1; Rare:46 | ||||
| chr5:177599979-177600159 | Common:3; Rare:55 |