| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:170026340-170026599 | Common:4; Rare:105 | ||||
| chr4:173369506-173369552 | Common:1; Rare:9 | ||||
| chr4:173369744-173369945 | Common:1; Rare:67 | ||||
| chr4:173370681-173371036 | Common:2; Rare:88 | ||||
| chr4:173530094-173530539 | Common:3; Rare:87 | ||||
| chr4:174283436-174283965 | Common:2; Rare:96 | ||||
| chr4:174522315-174522619 | Rare:98; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr4:174829220-174829412 | Common:1; Rare:39 | ||||
| chr4:176195566-176195722 | Common:1; Rare:56 | ||||
| chr4:176319637-176320042 | Common:4; Rare:126 | ||||
| chr4:177442156-177442198 | Rare:15 | ||||
| chr4:177442257-177442530 | Common:1; Rare:148; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
| chr4:182143819-182143963 | Common:2; Rare:32 | ||||
| chr4:182144193-182144220 | Common:3; Rare:6 | ||||
| chr4:182144418-182144719 | Common:3; Rare:93 |