| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:25914051-25914291 | Common:2; Rare:103 | ||||
| chr4:26320874-26321043 | Rare:58; Clinvar (benign):1 | ||||
| chr4:36281477-36281627 | Rare:25 | ||||
| chr4:37826548-37826748 | Common:5; Rare:76 | ||||
| chr4:38664211-38664352 | Common:1; Rare:44 | ||||
| chr4:39182202-39182548 | Rare:75; Clinvar:2 | ||||
| chr4:39458857-39459122 | Common:3; Rare:153; Clinvar:1; Clinvar (benign):5 | ||||
| chr4:39527383-39527755 | Common:2; Rare:91 | ||||
| chr4:39528192-39528291 | Common:2; Rare:26 | ||||
| chr4:39638835-39639140 | Common:1; Rare:112 | ||||
| chr4:39698022-39698181 | Common:1; Rare:65 | ||||
| chr4:39698675-39698870 | Rare:38 | ||||
| chr4:40056666-40056935 | Common:4; Rare:90 | ||||
| chr4:41990401-41990747 | Common:3; Rare:127 | ||||
| chr4:44678623-44678750 | Rare:56 |