| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:39276850-39277042 | Rare:36; Clinvar:1 | ||||
| chr4:39366240-39366464 | Common:2; Rare:71 | ||||
| chr4:39458658-39459118 | Common:6; Rare:192; Clinvar:1; Clinvar (benign):5 | ||||
| chr4:39527278-39527793 | Common:6; Rare:137 | ||||
| chr4:39527908-39528052 | Rare:34 | ||||
| chr4:39638184-39638357 | Common:1; Rare:34 | ||||
| chr4:39638831-39639190 | Common:1; Rare:137 | ||||
| chr4:39697983-39698307 | Common:1; Rare:118 | ||||
| chr4:39698310-39698390 | Rare:12 | ||||
| chr4:40056787-40056998 | Common:2; Rare:60 | ||||
| chr4:40196951-40197138 | Rare:28 | ||||
| chr4:40335249-40335359 | Common:2; Rare:26 | ||||
| chr4:40629418-40629596 | Common:1; Rare:29 | ||||
| chr4:40629817-40629939 | Common:1; Rare:32 | ||||
| chr4:40630099-40630229 | Common:1; Rare:17 |