| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:56655941-56656096 | Common:4; Rare:67; Clinvar (benign):1 | ||||
| chr4:56681282-56681421 | Common:1; Rare:19 | ||||
| chr4:56681523-56681598 | Rare:10 | ||||
| chr4:56821405-56821809 | Common:8; Rare:132 | ||||
| chr4:56907790-56907998 | Common:3; Rare:78 | ||||
| chr4:56977574-56977785 | Common:1; Rare:81 | ||||
| chr4:57023428-57023749 | Common:1; Rare:56 | ||||
| chr4:57109877-57110218 | Rare:112 | ||||
| chr4:57110366-57110536 | Common:1; Rare:55 | ||||
| chr4:67545358-67545742 | Common:2; Rare:91 | ||||
| chr4:67701115-67701415 | Common:4; Rare:140 | ||||
| chr4:68349734-68350224 | Common:3; Rare:174 | ||||
| chr4:70133507-70133622 | Rare:27 | ||||
| chr4:70334941-70335046 | Rare:27 | ||||
| chr4:70369990-70370117 | Rare:26 |