| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:15655322-15655473 | Common:1; Rare:65 | ||||
| chr4:15681458-15681766 | Common:3; Rare:101 | ||||
| chr4:15778134-15778407 | Rare:51 | ||||
| chr4:17577300-17577560 | Rare:123 | ||||
| chr4:17614537-17614670 | Common:2; Rare:60 | ||||
| chr4:17810618-17811065 | Common:4; Rare:139 | ||||
| chr4:18021734-18022008 | Common:2; Rare:91 | ||||
| chr4:20700280-20700499 | Common:1; Rare:97 | ||||
| chr4:24584408-24584725 | Common:1; Rare:98 | ||||
| chr4:25160392-25160732 | Common:3; Rare:97; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:25233841-25234050 | Rare:91 | ||||
| chr4:25312596-25312861 | Common:2; Rare:94 | ||||
| chr4:25376984-25377344 | Common:3; Rare:109 | ||||
| chr4:25861815-25862109 | Common:2; Rare:57 | ||||
| chr4:25863740-25864066 | Common:2; Rare:60 |