| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:143184865-143184973 | Common:3; Rare:42 | ||||
| chr4:144645931-144646166 | Common:1; Rare:64 | ||||
| chr4:145098156-145098343 | Rare:68 | ||||
| chr4:145619324-145619406 | Rare:32; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:145938392-145938578 | Common:1; Rare:40 | ||||
| chr4:147617248-147617444 | Common:1; Rare:44 | ||||
| chr4:150581710-150581935 | Rare:44 | ||||
| chr4:150582001-150582088 | Rare:13 | ||||
| chr4:152779729-152780172 | Common:2; Rare:113 | ||||
| chr4:158172592-158172711 | Rare:24 | ||||
| chr4:158671880-158672166 | Common:3; Rare:67; Clinvar:1 | ||||
| chr4:158672203-158672340 | Common:1; Rare:28; Clinvar:1; Clinvar (benign):1 | ||||
| chr4:169620381-169620697 | Common:2; Rare:110 | ||||
| chr4:173370692-173371012 | Common:2; Rare:81 | ||||
| chr4:174283631-174283953 | Common:1; Rare:62 |