| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:26320905-26321041 | Rare:47; Clinvar (benign):1 | ||||
| chr4:30719837-30720136 | Common:2; Rare:60 | ||||
| chr4:30722019-30722231 | Common:2; Rare:62 | ||||
| chr4:30722248-30722668 | Common:1; Rare:142 | ||||
| chr4:30722874-30723036 | Rare:39 | ||||
| chr4:37826590-37826744 | Common:1; Rare:60 | ||||
| chr4:37890992-37891128 | Common:1; Rare:42 | ||||
| chr4:37977143-37977463 | Rare:82 | ||||
| chr4:38867674-38867822 | Common:1; Rare:59 | ||||
| chr4:38868046-38868115 | Common:1; Rare:22 | ||||
| chr4:39458864-39459103 | Common:3; Rare:135; Clinvar (benign):4 | ||||
| chr4:39527342-39527761 | Common:4; Rare:106 | ||||
| chr4:39527881-39527987 | Rare:20 | ||||
| chr4:39528004-39528076 | Rare:16 | ||||
| chr4:39638823-39639140 | Common:1; Rare:115 |