| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:145098117-145098367 | Rare:81 | ||||
| chr4:145179573-145179973 | Rare:237 | ||||
| chr4:145180552-145180853 | Common:1; Rare:83 | ||||
| chr4:145481700-145481878 | Common:5; Rare:52 | ||||
| chr4:145619243-145619567 | Common:2; Rare:134; Clinvar:3; Clinvar (benign):1 | ||||
| chr4:145679570-145679930 | Common:3; Rare:67 | ||||
| chr4:145732885-145733059 | Rare:47 | ||||
| chr4:145938798-145938964 | Rare:44 | ||||
| chr4:145938981-145939131 | Common:2; Rare:66 | ||||
| chr4:146175602-146175785 | Common:1; Rare:61 | ||||
| chr4:146176014-146176414 | Common:6; Rare:140 | ||||
| chr4:146520873-146521670 | Common:5; Rare:218 | ||||
| chr4:146521837-146522019 | Rare:42 | ||||
| chr4:146522327-146522478 | Common:4; Rare:59 | ||||
| chr4:146945780-146946130 | Rare:78 |