| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:158671849-158672336 | Common:5; Rare:118; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:158723355-158723463 | Rare:48 | ||||
| chr4:163166832-163166968 | Common:2; Rare:44 | ||||
| chr4:163494468-163494745 | Common:2; Rare:109 | ||||
| chr4:164956832-164957042 | Common:4; Rare:72 | ||||
| chr4:164977648-164977738 | Rare:24 | ||||
| chr4:165112827-165113015 | Common:1; Rare:55 | ||||
| chr4:165327418-165327741 | Common:2; Rare:94 | ||||
| chr4:169010236-169010456 | Common:1; Rare:62 | ||||
| chr4:169612581-169612633 | Common:2; Rare:24; Clinvar:1; Clinvar (benign):1 | ||||
| chr4:169620329-169620604 | Common:2; Rare:108 | ||||
| chr4:169757880-169758063 | Rare:53 | ||||
| chr4:173333498-173333873 | Common:2; Rare:94 | ||||
| chr4:173334271-173334783 | Rare:128 | ||||
| chr4:173335210-173335362 | Common:2; Rare:38 |