| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:37826470-37827278 | Common:31; Rare:680 | ||||
| chr4:37977060-37977504 | Rare:366 | ||||
| chr4:38663395-38665161 | Common:28; Rare:2148 | ||||
| chr4:38856710-38857808 | Common:30; Rare:232 | ||||
| chr4:38867500-38867970 | Common:13; Rare:504 | ||||
| chr4:39032170-39032650 | Common:4; Rare:134 | ||||
| chr4:39032639-39033180 | Common:1; Rare:117 | ||||
| chr4:39044342-39045415 | Common:35; Rare:778 | ||||
| chr4:39182128-39182667 | Common:6; Rare:422; Clinvar:11; Clinvar (benign):4 | ||||
| chr4:39365612-39366012 | Common:1; Rare:73 | ||||
| chr4:39365915-39366069 | Common:2; Rare:35 | ||||
| chr4:39366058-39366620 | Common:10; Rare:533 | ||||
| chr4:39458054-39458717 | Common:3; Rare:303 | ||||
| chr4:39458697-39459330 | Common:25; Rare:1228; Clinvar:12; Clinvar (benign):38 | ||||
| chr4:39459329-39459729 | Common:1; Rare:164 |