| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:173528960-173529100 | Rare:97 | ||||
| chr4:173529245-173529670 | Common:3; Rare:226 | ||||
| chr4:173529657-173530229 | Rare:197 | ||||
| chr4:174283053-174283546 | Common:1; Rare:225 | ||||
| chr4:174283562-174284511 | Common:12; Rare:853 | ||||
| chr4:174284613-174285307 | Common:5; Rare:159 | ||||
| chr4:174522434-174522897 | Common:4; Rare:308; Clinvar:12; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr4:174523000-174523430 | Common:12; Rare:172 | ||||
| chr4:174829170-174829670 | Common:3; Rare:195 | ||||
| chr4:176195375-176195775 | Common:8; Rare:395 | ||||
| chr4:176277081-176277481 | Common:1; Rare:72 | ||||
| chr4:176319179-176320116 | Common:27; Rare:669 | ||||
| chr4:176320087-176320852 | Common:1; Rare:397 | ||||
| chr4:177309026-177310004 | Common:22; Rare:649 | ||||
| chr4:177310130-177310500 | Common:2; Rare:117 |