| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:169757875-169758069 | Rare:57 | ||||
| chr4:170026282-170026589 | Common:4; Rare:116 | ||||
| chr4:173333498-173333867 | Common:2; Rare:94 | ||||
| chr4:173334276-173334740 | Rare:117 | ||||
| chr4:173369796-173369935 | Common:1; Rare:46 | ||||
| chr4:173370674-173370975 | Common:2; Rare:78 | ||||
| chr4:173530221-173530353 | Rare:29 | ||||
| chr4:174283269-174283388 | Rare:20 | ||||
| chr4:174283410-174284005 | Common:2; Rare:110 | ||||
| chr4:174521957-174522186 | Common:5; Rare:56; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr4:174522189-174522686 | Common:2; Rare:139; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr4:174522785-174522908 | Common:1; Rare:18; Clinvar (benign):2 | ||||
| chr4:176319625-176320044 | Common:4; Rare:127 | ||||
| chr4:176320473-176320658 | Rare:58 | ||||
| chr4:177442012-177442225 | Common:2; Rare:65; Clinvar (benign):1 |