| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:172953966-172954098 | Common:1; Rare:24 | ||||
| chr5:173790871-173791044 | Common:3; Rare:40 | ||||
| chr5:175691178-175691276 | Rare:20 | ||||
| chr5:176411448-176411587 | Rare:24 | ||||
| chr5:176716410-176716502 | Rare:13 | ||||
| chr5:178206515-178206762 | Common:2; Rare:74 | ||||
| chr5:179530711-179530829 | Rare:31 | ||||
| chr5:179833258-179833780 | Common:9; Rare:175; Clinvar:4; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr5:179878450-179878706 | Common:3; Rare:56 | ||||
| chr5:180080819-180081074 | Common:5; Rare:74 | ||||
| chr5:180341911-180342099 | Rare:28 | ||||
| chr5:180467136-180467297 | Rare:26 | ||||
| chr5:180830178-180830484 | Common:2; Rare:88 | ||||
| chr5:180830881-180831055 | Common:1; Rare:52 | ||||
| chr5:180831567-180831679 | Common:2; Rare:47 |