| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:172834163-172834402 | Common:1; Rare:58 | ||||
| chr5:172959136-172959475 | Common:5; Rare:84 | ||||
| chr5:173328413-173328605 | Rare:36 | ||||
| chr5:176388558-176388809 | Common:4; Rare:97 | ||||
| chr5:176537856-176538127 | Common:1; Rare:87 | ||||
| chr5:177022635-177022741 | Rare:39 | ||||
| chr5:177133453-177133853 | Rare:145 | ||||
| chr5:177303691-177303934 | Common:3; Rare:104 | ||||
| chr5:177351650-177351767 | Rare:26 | ||||
| chr5:177516921-177517083 | Rare:57; Clinvar (pathogenic):1 | ||||
| chr5:178153825-178154170 | Rare:95; Clinvar:4; Clinvar (benign):1 | ||||
| chr5:178940990-178941239 | Common:1; Rare:68 | ||||
| chr5:179623613-179623976 | Common:4; Rare:132 | ||||
| chr5:179698646-179699091 | Common:4; Rare:150 | ||||
| chr5:179858798-179859040 | Rare:129 |