| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:48134183-48134367 | Rare:31 | ||||
| chr4:48269788-48270030 | Common:2; Rare:57 | ||||
| chr4:48341266-48341581 | Common:1; Rare:128 | ||||
| chr4:48780197-48780572 | Common:3; Rare:114 | ||||
| chr4:52659192-52659439 | Common:1; Rare:82 | ||||
| chr4:52862159-52862336 | Common:6; Rare:79 | ||||
| chr4:53365938-53366153 | Common:1; Rare:41 | ||||
| chr4:53377855-53377901 | Rare:11 | ||||
| chr4:54064381-54064463 | Rare:23 | ||||
| chr4:54657815-54657969 | Common:1; Rare:52 | ||||
| chr4:55346193-55346332 | Common:3; Rare:46; Clinvar:3; Clinvar (benign):2 | ||||
| chr4:55395858-55396225 | Common:2; Rare:121; Clinvar:2; Clinvar (benign):2 | ||||
| chr4:55546602-55546762 | Common:4; Rare:33 | ||||
| chr4:55546801-55547193 | Common:2; Rare:144 | ||||
| chr4:55948759-55948961 | Common:1; Rare:40 |