| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:15703011-15703138 | Common:1; Rare:28 | ||||
| chr4:16898517-16899008 | Common:14; Rare:85 | ||||
| chr4:17577293-17577550 | Common:1; Rare:122 | ||||
| chr4:17614548-17614660 | Common:2; Rare:49 | ||||
| chr4:17810598-17811155 | Common:5; Rare:163 | ||||
| chr4:25160370-25160731 | Common:3; Rare:108; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:25233843-25234089 | Rare:104 | ||||
| chr4:25914051-25914308 | Common:2; Rare:110 | ||||
| chr4:26320590-26320827 | Common:1; Rare:88 | ||||
| chr4:26320905-26321041 | Rare:47; Clinvar (benign):1 | ||||
| chr4:26860608-26860807 | Common:1; Rare:65 | ||||
| chr4:37826368-37826760 | Common:8; Rare:127 | ||||
| chr4:39182271-39182548 | Rare:64; Clinvar:2 | ||||
| chr4:39458796-39459112 | Common:3; Rare:161; Clinvar (benign):5 | ||||
| chr4:39527337-39527754 | Common:4; Rare:103 |