| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:102868819-102869059 | Common:2; Rare:80 | ||||
| chr4:105708636-105708843 | Common:1; Rare:68 | ||||
| chr4:106316179-106316580 | Common:5; Rare:126 | ||||
| chr4:107720185-107720490 | Common:7; Rare:123 | ||||
| chr4:107989690-107989860 | Common:2; Rare:74; Clinvar:2; Clinvar (benign):2 | ||||
| chr4:108620411-108620660 | Common:6; Rare:129 | ||||
| chr4:109703406-109703594 | Common:1; Rare:61 | ||||
| chr4:109730057-109730201 | Common:2; Rare:28 | ||||
| chr4:110198535-110198813 | Rare:81 | ||||
| chr4:112231593-112231831 | Common:2; Rare:74 | ||||
| chr4:112636869-112637182 | Common:1; Rare:86 | ||||
| chr4:112637322-112637508 | Common:3; Rare:54 | ||||
| chr4:119212408-119212730 | Common:2; Rare:98 | ||||
| chr4:120066754-120066906 | Common:1; Rare:48 | ||||
| chr4:120066927-120066955 | Common:1; Rare:6 |