| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:39697933-39698244 | Common:2; Rare:129 | ||||
| chr4:40056660-40056930 | Common:4; Rare:88 | ||||
| chr4:40630829-40630945 | Rare:28 | ||||
| chr4:41360680-41360874 | Common:1; Rare:52 | ||||
| chr4:41990390-41990563 | Common:1; Rare:63 | ||||
| chr4:44678352-44678706 | Common:1; Rare:130 | ||||
| chr4:47463635-47463860 | Common:3; Rare:71 | ||||
| chr4:48269790-48270000 | Common:2; Rare:49 | ||||
| chr4:48341300-48341617 | Common:1; Rare:125 | ||||
| chr4:48830834-48831223 | Common:1; Rare:123 | ||||
| chr4:51842822-51843245 | Common:1; Rare:128 | ||||
| chr4:51843382-51843695 | Rare:87 | ||||
| chr4:52038246-52038346 | Rare:39; Clinvar:6; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr4:52659211-52659420 | Common:1; Rare:72 | ||||
| chr4:53365987-53366222 | Rare:54 |