| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:15469659-15469912 | Common:1; Rare:53 | ||||
| chr4:15655230-15655473 | Common:2; Rare:97 | ||||
| chr4:15681720-15681869 | Common:1; Rare:56 | ||||
| chr4:17577316-17577550 | Rare:110 | ||||
| chr4:17614532-17614678 | Common:2; Rare:70 | ||||
| chr4:17810677-17810988 | Common:1; Rare:96 | ||||
| chr4:25160376-25160725 | Common:3; Rare:100; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:25233853-25234015 | Rare:67 | ||||
| chr4:25914051-25914332 | Common:2; Rare:120 | ||||
| chr4:26320874-26321043 | Rare:58; Clinvar (benign):1 | ||||
| chr4:26860624-26860812 | Common:2; Rare:63 | ||||
| chr4:37826561-37826729 | Common:2; Rare:60 | ||||
| chr4:37977208-37977463 | Rare:59 | ||||
| chr4:38664211-38664306 | Rare:32 | ||||
| chr4:39182328-39182548 | Rare:48; Clinvar:2 |