| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:177402397-177402797 | Rare:212; Clinvar:1 | ||||
| chr5:177404230-177404720 | Common:2; Rare:155; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr5:177425760-177426080 | Common:1; Rare:78 | ||||
| chr5:177446480-177446970 | Common:2; Rare:130 | ||||
| chr5:177447019-177447177 | Common:1; Rare:39 | ||||
| chr5:177466797-177467754 | Common:4; Rare:494 | ||||
| chr5:177472840-177472994 | Rare:47 | ||||
| chr5:177473200-177473480 | Rare:131 | ||||
| chr5:177473616-177473799 | Common:1; Rare:59 | ||||
| chr5:177496853-177497110 | Common:4; Rare:57 | ||||
| chr5:177497542-177497894 | Common:1; Rare:122 | ||||
| chr5:177516901-177517256 | Common:3; Rare:115; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr5:177553692-177554092 | Common:3; Rare:175 | ||||
| chr5:177554555-177554749 | Common:2; Rare:67 | ||||
| chr5:177592080-177592290 | Common:2; Rare:95 |