| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:153788407-153788737 | Common:2; Rare:104 | ||||
| chr4:153789081-153789222 | Rare:25 | ||||
| chr4:154743755-154744002 | Rare:84 | ||||
| chr4:158671830-158672313 | Common:5; Rare:121; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:158723202-158723463 | Common:2; Rare:112 | ||||
| chr4:163166826-163166954 | Common:2; Rare:41 | ||||
| chr4:163494679-163494769 | Rare:40 | ||||
| chr4:164876763-164877340 | Common:4; Rare:102 | ||||
| chr4:165112818-165113022 | Common:1; Rare:58 | ||||
| chr4:165327422-165327741 | Common:2; Rare:93 | ||||
| chr4:169010022-169010378 | Common:6; Rare:119 | ||||
| chr4:169271048-169271146 | Common:1; Rare:33 | ||||
| chr4:169620260-169620599 | Common:2; Rare:122 | ||||
| chr4:169757873-169758080 | Rare:60 | ||||
| chr4:173333498-173333875 | Common:2; Rare:95 |