| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:25234117-25234256 | Common:2; Rare:40 | ||||
| chr4:25914051-25914275 | Common:2; Rare:98 | ||||
| chr4:26319372-26319878 | Rare:138 | ||||
| chr4:26320450-26321082 | Common:1; Rare:218; Clinvar (benign):1 | ||||
| chr4:26321502-26321632 | Common:1; Rare:36 | ||||
| chr4:26857327-26857814 | Common:4; Rare:130 | ||||
| chr4:26857838-26858097 | Common:1; Rare:60 | ||||
| chr4:26860560-26860856 | Common:3; Rare:100 | ||||
| chr4:30720244-30720425 | Common:1; Rare:48 | ||||
| chr4:37826509-37826730 | Common:6; Rare:80 | ||||
| chr4:38664133-38664200 | Common:1; Rare:16 | ||||
| chr4:38664219-38664278 | Rare:16 | ||||
| chr4:38664832-38665241 | Common:2; Rare:104 | ||||
| chr4:38867682-38867822 | Common:1; Rare:58 | ||||
| chr4:39182202-39182560 | Common:1; Rare:81; Clinvar:2; Clinvar (benign):1 |