| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:105708649-105708874 | Common:3; Rare:73 | ||||
| chr4:106315537-106315586 | Rare:10 | ||||
| chr4:106316173-106316664 | Common:5; Rare:154 | ||||
| chr4:107720165-107720511 | Common:7; Rare:139 | ||||
| chr4:107989679-107989927 | Common:6; Rare:114; Clinvar:4; Clinvar (benign):5 | ||||
| chr4:108620380-108620647 | Common:6; Rare:135 | ||||
| chr4:109433750-109433913 | Common:1; Rare:57 | ||||
| chr4:109703412-109703630 | Common:1; Rare:70 | ||||
| chr4:109815458-109815798 | Common:1; Rare:90 | ||||
| chr4:110198535-110198795 | Rare:75 | ||||
| chr4:112231591-112231947 | Common:2; Rare:103 | ||||
| chr4:112285757-112285976 | Rare:68 | ||||
| chr4:112636875-112637181 | Rare:83 | ||||
| chr4:112637346-112637570 | Common:3; Rare:66 | ||||
| chr4:113049450-113049689 | Common:1; Rare:41 |