| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:37453740-37454130 | Common:1; Rare:114 | ||||
| chr4:37826300-37826750 | Common:8; Rare:136 | ||||
| chr4:37890869-37891531 | Common:12; Rare:299 | ||||
| chr4:37977192-37977328 | Rare:40 | ||||
| chr4:37977412-37977812 | Rare:132 | ||||
| chr4:38109855-38110206 | Common:1; Rare:48 | ||||
| chr4:38663927-38664262 | Common:2; Rare:114 | ||||
| chr4:38867654-38867814 | Common:1; Rare:62 | ||||
| chr4:39044411-39044891 | Common:6; Rare:136 | ||||
| chr4:39045107-39045507 | Common:7; Rare:171 | ||||
| chr4:39062836-39062961 | Rare:37 | ||||
| chr4:39182101-39182546 | Common:2; Rare:95; Clinvar:2 | ||||
| chr4:39366064-39366488 | Common:3; Rare:130 | ||||
| chr4:39458831-39459118 | Common:3; Rare:158; Clinvar:1; Clinvar (benign):5 | ||||
| chr4:39527320-39527780 | Common:4; Rare:124 |