| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:177311882-177312048 | Common:1; Rare:45 | ||||
| chr5:177312265-177312538 | Rare:83 | ||||
| chr5:177402864-177402932 | Rare:14 | ||||
| chr5:177460435-177460708 | Common:1; Rare:91 | ||||
| chr5:177516872-177517100 | Common:2; Rare:89; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr5:178153745-178154110 | Rare:118; Clinvar:5; Clinvar (benign):1 | ||||
| chr5:178204339-178204534 | Common:3; Rare:68 | ||||
| chr5:178859881-178860007 | Rare:38 | ||||
| chr5:178895805-178895956 | Rare:57 | ||||
| chr5:178940924-178941239 | Common:1; Rare:85 | ||||
| chr5:179023670-179023852 | Common:2; Rare:56 | ||||
| chr5:179060249-179060624 | Common:3; Rare:90 | ||||
| chr5:179559534-179559814 | Common:1; Rare:79 | ||||
| chr5:179623590-179623991 | Common:4; Rare:144 | ||||
| chr5:179698366-179698432 | Common:1; Rare:21 |