| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:17512055-17512369 | Common:4; Rare:101; Clinvar:2; Clinvar (benign):3 | ||||
| chr4:17614553-17614647 | Common:2; Rare:40 | ||||
| chr4:17810664-17811080 | Common:4; Rare:133 | ||||
| chr4:20700270-20700540 | Common:2; Rare:114 | ||||
| chr4:25160410-25160710 | Common:3; Rare:84; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:25914051-25914297 | Common:2; Rare:103 | ||||
| chr4:26320917-26321041 | Rare:43 | ||||
| chr4:26583981-26584124 | Rare:28 | ||||
| chr4:30720268-30720422 | Rare:41 | ||||
| chr4:37826449-37826729 | Common:8; Rare:93 | ||||
| chr4:38867588-38867822 | Common:2; Rare:83 | ||||
| chr4:39182204-39182548 | Rare:74; Clinvar:2 | ||||
| chr4:39458849-39459112 | Common:3; Rare:149; Clinvar (benign):5 | ||||
| chr4:39527426-39527755 | Common:2; Rare:83 | ||||
| chr4:39527951-39527997 | Rare:10 |