| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:41360570-41360843 | Common:2; Rare:79 | ||||
| chr4:41990401-41990580 | Common:1; Rare:65 | ||||
| chr4:44678573-44678706 | Rare:57 | ||||
| chr4:44726547-44726659 | Rare:48 | ||||
| chr4:47485198-47485359 | Common:1; Rare:58 | ||||
| chr4:48016624-48016794 | Common:1; Rare:50 | ||||
| chr4:48269802-48270000 | Common:1; Rare:44 | ||||
| chr4:48341243-48341560 | Common:2; Rare:128 | ||||
| chr4:48780182-48780572 | Common:3; Rare:120 | ||||
| chr4:53458351-53458729 | Rare:64 | ||||
| chr4:53591451-53591640 | Common:1; Rare:39 | ||||
| chr4:53652442-53652692 | Common:2; Rare:37 | ||||
| chr4:54064410-54064436 | Rare:5 | ||||
| chr4:54228979-54229370 | Common:1; Rare:86; Clinvar (benign):4 | ||||
| chr4:54657815-54658054 | Common:2; Rare:87; Clinvar:2; Clinvar (benign):2 |