| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:17810651-17811006 | Common:2; Rare:111 | ||||
| chr4:24795447-24795592 | Common:1; Rare:29 | ||||
| chr4:25160388-25160725 | Common:3; Rare:95; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:25233856-25234074 | Rare:94 | ||||
| chr4:26320450-26320814 | Common:1; Rare:108 | ||||
| chr4:26430391-26430856 | Common:1; Rare:97 | ||||
| chr4:37826637-37826724 | Common:1; Rare:35 | ||||
| chr4:39458843-39459075 | Common:3; Rare:127; Clinvar (benign):1 | ||||
| chr4:39527359-39527754 | Common:2; Rare:93 | ||||
| chr4:39638850-39639140 | Common:1; Rare:109 | ||||
| chr4:52659273-52659402 | Common:1; Rare:45 | ||||
| chr4:56435554-56435974 | Common:4; Rare:129 | ||||
| chr4:56467552-56467660 | Common:2; Rare:43; Clinvar (benign):4 | ||||
| chr4:56977529-56977757 | Common:2; Rare:88 | ||||
| chr4:67701130-67701401 | Common:4; Rare:123 |