| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:173370687-173370982 | Common:2; Rare:74 | ||||
| chr4:173371192-173371360 | Common:3; Rare:58 | ||||
| chr4:173530156-173530487 | Common:2; Rare:68 | ||||
| chr4:174283342-174283394 | Rare:10 | ||||
| chr4:174283549-174283967 | Common:1; Rare:81 | ||||
| chr4:174284262-174284391 | Common:1; Rare:29 | ||||
| chr4:174522120-174522137 | Rare:7 | ||||
| chr4:174522227-174522762 | Common:2; Rare:142; Clinvar:5; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr4:174522767-174522856 | Common:1; Rare:17; Clinvar (benign):1 | ||||
| chr4:174522864-174523031 | Rare:26; Clinvar (benign):1 | ||||
| chr4:176319721-176320083 | Common:5; Rare:120 | ||||
| chr4:177442375-177442530 | Rare:94; Clinvar:2 | ||||
| chr4:182917319-182917594 | Common:4; Rare:89 | ||||
| chr4:183444351-183444725 | Common:2; Rare:160 | ||||
| chr4:183504522-183504814 | Common:2; Rare:95 |