| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:141769756-141769834 | Rare:13 | ||||
| chr3:156373155-156373485 | Rare:60 | ||||
| chr3:157089133-157089325 | Rare:66 | ||||
| chr3:157174831-157175263 | Common:3; Rare:185 | ||||
| chr3:159005279-159005529 | Common:2; Rare:45 | ||||
| chr3:160515202-160515489 | Common:1; Rare:60 | ||||
| chr3:165572735-165572898 | Common:4; Rare:60 | ||||
| chr3:165874618-165874768 | Common:1; Rare:31 | ||||
| chr3:168096505-168096663 | Rare:21 | ||||
| chr3:169510425-169510733 | Common:2; Rare:32 | ||||
| chr3:169764970-169765252 | Common:1; Rare:106; Clinvar:7; Clinvar (pathogenic):4 | ||||
| chr3:174211232-174211481 | Common:2; Rare:51 | ||||
| chr3:177358375-177358789 | Common:3; Rare:92 | ||||
| chr3:177359321-177359478 | Rare:43 | ||||
| chr3:177359906-177360136 | Rare:54 |