| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:54064507-54064782 | Common:5; Rare:179 | ||||
| chr4:55346202-55346394 | Common:5; Rare:121; Clinvar:7; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr4:55395380-55395690 | Rare:120 | ||||
| chr4:55395783-55396209 | Common:7; Rare:207; Clinvar:4; Clinvar (benign):2 | ||||
| chr4:55545710-55546140 | Common:3; Rare:109 | ||||
| chr4:55546540-55546780 | Common:8; Rare:83 | ||||
| chr4:55546795-55546998 | Common:2; Rare:79 | ||||
| chr4:55547110-55547550 | Common:4; Rare:231 | ||||
| chr4:55853370-55853804 | Rare:194 | ||||
| chr4:55948648-55948974 | Common:3; Rare:107 | ||||
| chr4:55949032-55949432 | Common:2; Rare:130 | ||||
| chr4:56048985-56049160 | Common:1; Rare:56 | ||||
| chr4:56387010-56387340 | Rare:138 | ||||
| chr4:56387361-56387556 | Rare:104 | ||||
| chr4:56435434-56435810 | Common:10; Rare:224 |