| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:145619032-145619534 | Common:4; Rare:182; Clinvar:3; Clinvar (benign):1 | ||||
| chr4:145732901-145733306 | Common:3; Rare:120 | ||||
| chr4:145870134-145870328 | Rare:47 | ||||
| chr4:145938136-145938283 | Rare:25 | ||||
| chr4:145938773-145939056 | Common:1; Rare:76 | ||||
| chr4:146175620-146175809 | Common:1; Rare:62 | ||||
| chr4:146521668-146521680 | Rare:6 | ||||
| chr4:146522267-146522557 | Common:6; Rare:80 | ||||
| chr4:147617179-147617519 | Common:1; Rare:77 | ||||
| chr4:147617606-147617712 | Rare:17 | ||||
| chr4:147684057-147684396 | Common:1; Rare:118 | ||||
| chr4:147731490-147731688 | Common:2; Rare:43 | ||||
| chr4:147731713-147732250 | Common:1; Rare:145 | ||||
| chr4:147732253-147732359 | Rare:51 | ||||
| chr4:148442509-148442764 | Rare:76 |