| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:163508070-163508480 | Rare:134 | ||||
| chr3:163513298-163513850 | Common:3; Rare:170 | ||||
| chr3:163526340-163526690 | Common:2; Rare:92 | ||||
| chr3:163543708-163544306 | Rare:163 | ||||
| chr3:163556751-163557728 | Rare:264 | ||||
| chr3:163560361-163560870 | Common:3; Rare:151 | ||||
| chr3:163716765-163717370 | Common:3; Rare:147 | ||||
| chr3:163722390-163722906 | Common:5; Rare:140 | ||||
| chr3:163809582-163810033 | Common:11; Rare:252 | ||||
| chr3:163821944-163822135 | Common:2; Rare:32 | ||||
| chr3:163828820-163829229 | Common:2; Rare:148 | ||||
| chr3:163829203-163829603 | Common:1; Rare:113 | ||||
| chr3:169764831-169765258 | Common:2; Rare:281; Clinvar:32; Clinvar (benign):1; Clinvar (pathogenic):11 | ||||
| chr3:170356640-170357010 | Common:5; Rare:234 | ||||
| chr3:171811478-171811878 | Common:4; Rare:100 |