| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:175871253-175871685 | Common:3; Rare:140 | ||||
| chr5:175968204-175968428 | Common:2; Rare:38 | ||||
| chr5:176388550-176388821 | Common:4; Rare:111 | ||||
| chr5:176416368-176416652 | Common:1; Rare:83 | ||||
| chr5:176448221-176448410 | Common:1; Rare:70 | ||||
| chr5:176610021-176610276 | Common:3; Rare:99 | ||||
| chr5:177006680-177006996 | Common:2; Rare:98 | ||||
| chr5:177022628-177022807 | Rare:69 | ||||
| chr5:177133453-177133845 | Rare:142 | ||||
| chr5:177303655-177304075 | Common:4; Rare:160 | ||||
| chr5:177351643-177351951 | Rare:79 | ||||
| chr5:177516881-177517093 | Common:2; Rare:85; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr5:177599970-177600179 | Common:3; Rare:64; Clinvar (benign):1 | ||||
| chr5:178153751-178154103 | Rare:112; Clinvar:5; Clinvar (benign):1 | ||||
| chr5:178859857-178860086 | Common:3; Rare:63 |