| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:158671830-158672393 | Common:5; Rare:143; Clinvar:3; Clinvar (benign):1 | ||||
| chr4:158723339-158723463 | Common:2; Rare:56 | ||||
| chr4:159267042-159267183 | Rare:21 | ||||
| chr4:162163927-162164133 | Common:1; Rare:49 | ||||
| chr4:163332538-163332618 | Common:1; Rare:12 | ||||
| chr4:164383383-164383583 | Common:2; Rare:52 | ||||
| chr4:164956859-164957019 | Common:2; Rare:52 | ||||
| chr4:165112825-165113015 | Common:1; Rare:56 | ||||
| chr4:165327411-165327748 | Common:2; Rare:99 | ||||
| chr4:165378692-165379363 | Common:3; Rare:150 | ||||
| chr4:168480471-168480524 | Rare:11 | ||||
| chr4:169010233-169010474 | Common:1; Rare:73 | ||||
| chr4:169620381-169620723 | Common:2; Rare:117 | ||||
| chr4:169660150-169660282 | Rare:21 | ||||
| chr4:169757842-169758074 | Common:1; Rare:72 |