| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:146521665-146522150 | Rare:280 | ||||
| chr4:146522168-146522568 | Common:31; Rare:490 | ||||
| chr4:147617103-147617503 | Common:7; Rare:425 | ||||
| chr4:147683868-147684774 | Common:9; Rare:703 | ||||
| chr4:147731720-147732330 | Common:1; Rare:184 | ||||
| chr4:148442391-148442791 | Rare:462; Clinvar:9; Clinvar (benign):4 | ||||
| chr4:150302496-150302896 | Rare:122; Clinvar:1; Clinvar (benign):2 | ||||
| chr4:150315221-150315621 | Common:4; Rare:93; Clinvar:3 | ||||
| chr4:151014646-151016098 | Common:6; Rare:1179 | ||||
| chr4:151016139-151016405 | Common:1; Rare:52 | ||||
| chr4:151099150-151099765 | Common:15; Rare:578 | ||||
| chr4:151099700-151099890 | Rare:46 | ||||
| chr4:151099980-151100676 | Common:1; Rare:153 | ||||
| chr4:151408840-151409260 | Common:15; Rare:338 | ||||
| chr4:151760134-151760536 | Common:2; Rare:62 |