| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:4290118-4290237 | Common:1; Rare:44 | ||||
| chr4:4541975-4542319 | Common:2; Rare:121 | ||||
| chr4:5826198-5826446 | Common:4; Rare:67 | ||||
| chr4:6269602-6269885 | Common:2; Rare:96; Clinvar:1 | ||||
| chr4:6640565-6640721 | Common:2; Rare:62 | ||||
| chr4:6709782-6709998 | Common:2; Rare:63 | ||||
| chr4:6987002-6987281 | Common:2; Rare:85 | ||||
| chr4:8440715-8440750 | Rare:10 | ||||
| chr4:15681423-15681757 | Common:3; Rare:105 | ||||
| chr4:15702990-15703114 | Common:1; Rare:22 | ||||
| chr4:17614568-17614651 | Common:2; Rare:38 | ||||
| chr4:25160392-25160732 | Common:3; Rare:97; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:25233853-25234061 | Rare:90 | ||||
| chr4:25914051-25914268 | Common:2; Rare:96 | ||||
| chr4:26857454-26857740 | Common:4; Rare:80 |