| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:169765032-169765189 | Rare:70; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr3:170284358-170284601 | Common:1; Rare:49 | ||||
| chr3:170300336-170300392 | Rare:9 | ||||
| chr3:170423881-170424123 | Common:7; Rare:32 | ||||
| chr3:170426015-170426148 | Common:1; Rare:20 | ||||
| chr3:170740507-170740781 | Rare:26 | ||||
| chr3:170894310-170894615 | Rare:69 | ||||
| chr3:172043376-172043442 | Rare:13 | ||||
| chr3:172058205-172058402 | Common:2; Rare:39 | ||||
| chr3:172062929-172063224 | Common:1; Rare:65 | ||||
| chr3:172066783-172067004 | Common:1; Rare:43 | ||||
| chr3:172180895-172180975 | Common:1; Rare:16 | ||||
| chr3:172257690-172257964 | Common:1; Rare:56 | ||||
| chr3:172381026-172381462 | Common:3; Rare:80 | ||||
| chr3:172702846-172703083 | Common:1; Rare:46 |