| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:173370661-173370982 | Common:2; Rare:82 | ||||
| chr4:173399105-173399385 | Common:1; Rare:51 | ||||
| chr4:173530072-173530758 | Common:3; Rare:132 | ||||
| chr4:174283111-174283332 | Rare:32 | ||||
| chr4:174283611-174284028 | Common:1; Rare:93 | ||||
| chr4:174522429-174522572 | Rare:49; Clinvar (pathogenic):1 | ||||
| chr4:176195569-176195722 | Common:1; Rare:56 | ||||
| chr4:176319721-176320048 | Common:4; Rare:112 | ||||
| chr4:177309766-177309948 | Common:2; Rare:57 | ||||
| chr4:177442141-177442184 | Rare:18 | ||||
| chr4:177442349-177442530 | Rare:109; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr4:182917287-182917554 | Common:4; Rare:86 | ||||
| chr4:183444416-183444702 | Common:2; Rare:133 | ||||
| chr4:183504523-183504803 | Common:1; Rare:94 | ||||
| chr4:183659080-183659439 | Common:1; Rare:113 |