| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:337532-337837 | Common:1; Rare:73 | ||||
| chr4:499117-499389 | Common:3; Rare:117; Clinvar (benign):1 | ||||
| chr4:663611-663760 | Rare:52 | ||||
| chr4:674211-674542 | Common:1; Rare:151 | ||||
| chr4:705578-705846 | Rare:87 | ||||
| chr4:932259-932535 | Common:2; Rare:108 | ||||
| chr4:1289688-1289913 | Common:1; Rare:73 | ||||
| chr4:2041942-2042057 | Rare:51 | ||||
| chr4:2468878-2469180 | Common:4; Rare:117 | ||||
| chr4:2746170-2746498 | Rare:61 | ||||
| chr4:2755993-2756024 | Rare:9 | ||||
| chr4:2812190-2812381 | Rare:32 | ||||
| chr4:2843705-2844019 | Common:3; Rare:112 | ||||
| chr4:2934777-2934886 | Common:1; Rare:50 | ||||
| chr4:2963317-2963595 | Common:2; Rare:104 |