| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:158671818-158672313 | Common:5; Rare:126; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:158723202-158723467 | Common:2; Rare:115 | ||||
| chr4:163166860-163166946 | Common:2; Rare:26 | ||||
| chr4:165112818-165113015 | Common:1; Rare:57 | ||||
| chr4:165327412-165327741 | Common:2; Rare:95 | ||||
| chr4:168318727-168318893 | Common:1; Rare:35 | ||||
| chr4:169010236-169010474 | Common:1; Rare:73 | ||||
| chr4:169620391-169620725 | Common:2; Rare:115 | ||||
| chr4:169620842-169620950 | Rare:21 | ||||
| chr4:169757842-169758074 | Common:1; Rare:72 | ||||
| chr4:173168200-173168280 | Common:1; Rare:17 | ||||
| chr4:173168714-173168844 | Common:2; Rare:50 | ||||
| chr4:173334261-173334692 | Rare:110 | ||||
| chr4:173369744-173369935 | Common:1; Rare:63 | ||||
| chr4:173370668-173370982 | Common:2; Rare:79 |