| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:932302-932480 | Common:2; Rare:73 | ||||
| chr4:2468820-2469159 | Common:3; Rare:125 | ||||
| chr4:4248209-4248311 | Common:2; Rare:36 | ||||
| chr4:4290083-4290291 | Common:5; Rare:87 | ||||
| chr4:4541976-4542165 | Common:1; Rare:78 | ||||
| chr4:6987028-6987268 | Common:1; Rare:72 | ||||
| chr4:11429160-11429231 | Rare:14 | ||||
| chr4:15681458-15681854 | Common:3; Rare:140 | ||||
| chr4:17810701-17811039 | Common:3; Rare:105 | ||||
| chr4:25160405-25160727 | Common:3; Rare:90; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:37826571-37826729 | Common:1; Rare:57 | ||||
| chr4:38867612-38867826 | Common:2; Rare:79 | ||||
| chr4:39458864-39459122 | Common:3; Rare:146; Clinvar:1; Clinvar (benign):5 | ||||
| chr4:39527426-39527731 | Common:2; Rare:75 | ||||
| chr4:39638838-39639158 | Common:1; Rare:117 |