| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:37826544-37826723 | Common:6; Rare:64 | ||||
| chr4:37977189-37977442 | Rare:65 | ||||
| chr4:39458889-39459075 | Common:2; Rare:97; Clinvar (benign):1 | ||||
| chr4:39527426-39527754 | Common:2; Rare:82 | ||||
| chr4:39638847-39639140 | Common:1; Rare:109 | ||||
| chr4:39697930-39698174 | Common:2; Rare:106 | ||||
| chr4:48016541-48016813 | Common:2; Rare:82 | ||||
| chr4:48830935-48831223 | Common:1; Rare:86 | ||||
| chr4:53366022-53366222 | Rare:47 | ||||
| chr4:56387457-56387513 | Rare:19 | ||||
| chr4:56435473-56435736 | Common:5; Rare:98 | ||||
| chr4:56467552-56467699 | Common:2; Rare:61; Clinvar (benign):5 | ||||
| chr4:67701121-67701391 | Common:4; Rare:122 | ||||
| chr4:70688464-70688567 | Common:2; Rare:25 | ||||
| chr4:73620423-73620477 | Rare:24 |