| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:338024-338112 | Common:2; Rare:27 | ||||
| chr4:473854-473958 | Rare:31 | ||||
| chr4:474054-474357 | Common:3; Rare:106 | ||||
| chr4:499026-499390 | Common:3; Rare:148; Clinvar (benign):1 | ||||
| chr4:663576-663842 | Rare:105; Clinvar:1 | ||||
| chr4:664136-664327 | Common:1; Rare:76; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:674185-674629 | Common:4; Rare:200 | ||||
| chr4:689373-689423 | Rare:16 | ||||
| chr4:705553-706048 | Common:2; Rare:161 | ||||
| chr4:932212-932568 | Common:2; Rare:130 | ||||
| chr4:973487-973821 | Common:7; Rare:104 | ||||
| chr4:986853-987098 | Common:1; Rare:78; Clinvar:2 | ||||
| chr4:987260-987302 | Rare:14 | ||||
| chr4:1200798-1200957 | Common:2; Rare:45 | ||||
| chr4:1201525-1201870 | Rare:95 |