| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:705589-705927 | Common:1; Rare:113 | ||||
| chr4:932162-932493 | Common:2; Rare:125 | ||||
| chr4:986929-987150 | Common:2; Rare:72; Clinvar:3; Clinvar (benign):2 | ||||
| chr4:1113501-1113627 | Common:2; Rare:48 | ||||
| chr4:1171123-1171464 | Common:2; Rare:149 | ||||
| chr4:2468897-2469163 | Common:2; Rare:98 | ||||
| chr4:2825110-2825394 | Common:1; Rare:74; Clinvar:1; Clinvar (benign):1 | ||||
| chr4:2843679-2844011 | Common:3; Rare:123 | ||||
| chr4:2934767-2934910 | Common:1; Rare:66 | ||||
| chr4:3292747-3293079 | Common:2; Rare:126 | ||||
| chr4:3386016-3386286 | Common:3; Rare:41 | ||||
| chr4:3532211-3532263 | Rare:18; Clinvar (pathogenic):2 | ||||
| chr4:4248201-4248266 | Common:1; Rare:27 | ||||
| chr4:4290110-4290277 | Common:3; Rare:69 | ||||
| chr4:4541937-4542186 | Common:1; Rare:101 |