| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:25160392-25160741 | Common:3; Rare:100; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:25233853-25234050 | Rare:87 | ||||
| chr4:25914051-25914297 | Common:2; Rare:103 | ||||
| chr4:26319391-26319836 | Rare:116 | ||||
| chr4:26320623-26320832 | Common:1; Rare:85 | ||||
| chr4:26320905-26321057 | Rare:55; Clinvar (benign):1 | ||||
| chr4:26583981-26584131 | Rare:31 | ||||
| chr4:30719965-30720083 | Common:1; Rare:24 | ||||
| chr4:37826534-37826728 | Common:6; Rare:69 | ||||
| chr4:37977173-37977447 | Rare:67 | ||||
| chr4:38867606-38867826 | Common:2; Rare:82 | ||||
| chr4:38868135-38868446 | Rare:65 | ||||
| chr4:39182172-39182510 | Rare:73; Clinvar:1 | ||||
| chr4:39366324-39366398 | Rare:24 | ||||
| chr4:39458857-39459109 | Common:3; Rare:145; Clinvar (benign):5 |