| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:53365627-53365665 | Rare:11 | ||||
| chr4:55395830-55395991 | Common:2; Rare:46; Clinvar:2 | ||||
| chr4:56435473-56435974 | Common:6; Rare:165 | ||||
| chr4:56467359-56467686 | Common:3; Rare:108; Clinvar (benign):4 | ||||
| chr4:56977518-56977660 | Common:1; Rare:68 | ||||
| chr4:57110083-57110248 | Rare:53 | ||||
| chr4:67701078-67701423 | Common:4; Rare:161 | ||||
| chr4:70688874-70688926 | Rare:13 | ||||
| chr4:73258778-73258918 | Rare:40 | ||||
| chr4:73998175-73998819 | Common:2; Rare:192 | ||||
| chr4:74038672-74039111 | Rare:110 | ||||
| chr4:74099165-74099429 | Common:2; Rare:60 | ||||
| chr4:74445011-74445138 | Rare:26 | ||||
| chr4:75514267-75514483 | Common:1; Rare:72 | ||||
| chr4:75724367-75724859 | Common:2; Rare:156 |