| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:48269807-48269981 | Common:1; Rare:35 | ||||
| chr4:48341333-48341614 | Common:1; Rare:113 | ||||
| chr4:48341777-48342014 | Rare:68 | ||||
| chr4:48780236-48780572 | Common:2; Rare:101 | ||||
| chr4:52038230-52038357 | Rare:53; Clinvar:9; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
| chr4:52659211-52659439 | Common:1; Rare:77 | ||||
| chr4:52862132-52862320 | Common:7; Rare:88 | ||||
| chr4:53458530-53458580 | Rare:6 | ||||
| chr4:54657787-54658037 | Common:2; Rare:92; Clinvar:1; Clinvar (benign):2 | ||||
| chr4:55395840-55395978 | Common:1; Rare:36; Clinvar:2 | ||||
| chr4:55396050-55396233 | Common:1; Rare:66; Clinvar (benign):2 | ||||
| chr4:55546805-55547232 | Common:4; Rare:159 | ||||
| chr4:56387423-56387528 | Rare:35 | ||||
| chr4:56435482-56435758 | Common:5; Rare:100 | ||||
| chr4:56467521-56467699 | Common:2; Rare:73; Clinvar (benign):5 |