| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:157174851-157175255 | Common:3; Rare:176 | ||||
| chr3:159732274-159732390 | Common:1; Rare:19 | ||||
| chr3:159765683-159765988 | Rare:61 | ||||
| chr3:160226651-160226704 | Rare:9 | ||||
| chr3:164451355-164451416 | Common:1; Rare:10 | ||||
| chr3:169765029-169765267 | Rare:90; Clinvar:3; Clinvar (pathogenic):2 | ||||
| chr3:184183991-184184239 | Common:2; Rare:50 | ||||
| chr3:184324166-184324245 | Common:1; Rare:24 | ||||
| chr3:187742395-187742648 | Common:1; Rare:44 | ||||
| chr3:187742814-187743091 | Common:3; Rare:58 | ||||
| chr3:187743171-187743348 | Rare:41 | ||||
| chr3:187744410-187744739 | Common:4; Rare:139 | ||||
| chr3:188211513-188211762 | Common:2; Rare:47 | ||||
| chr3:188266104-188266334 | Rare:49 | ||||
| chr3:188296832-188296950 | Rare:22 |