| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:146269387-146269636 | Rare:35 | ||||
| chr4:146271528-146271763 | Common:3; Rare:33 | ||||
| chr4:146273230-146273468 | Rare:40 | ||||
| chr4:146520959-146521107 | Rare:24 | ||||
| chr4:146522859-146523043 | Rare:41 | ||||
| chr4:147683231-147683402 | Rare:32 | ||||
| chr4:147732621-147732706 | Common:1; Rare:20 | ||||
| chr4:147733461-147733552 | Common:2; Rare:18 | ||||
| chr4:147734725-147734810 | Rare:11 | ||||
| chr4:147780248-147780332 | Rare:21 | ||||
| chr4:147780596-147780797 | Rare:26 | ||||
| chr4:147794882-147795158 | Common:1; Rare:50 | ||||
| chr4:147800005-147800329 | Common:1; Rare:66 | ||||
| chr4:151014567-151014641 | Rare:19; Clinvar:1 | ||||
| chr4:151014649-151014730 | Rare:19 |