| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:499141-499324 | Common:2; Rare:67 | ||||
| chr4:674210-674596 | Common:4; Rare:180 | ||||
| chr4:932174-932492 | Common:2; Rare:122 | ||||
| chr4:993384-993560 | Common:5; Rare:30 | ||||
| chr4:993866-993917 | Common:3; Rare:16 | ||||
| chr4:1289659-1289980 | Common:1; Rare:114 | ||||
| chr4:2468880-2469167 | Common:4; Rare:108 | ||||
| chr4:2792874-2793123 | Common:2; Rare:69 | ||||
| chr4:2843678-2843994 | Common:3; Rare:117 | ||||
| chr4:2934777-2934910 | Common:1; Rare:64 | ||||
| chr4:2963309-2963587 | Common:2; Rare:103 | ||||
| chr4:3385002-3385363 | Common:3; Rare:84 | ||||
| chr4:3441870-3442117 | Common:1; Rare:89 | ||||
| chr4:3532223-3532343 | Rare:42; Clinvar (pathogenic):1 | ||||
| chr4:4248169-4248266 | Common:3; Rare:48 |