| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:107824370-107825020 | Common:3; Rare:221 | ||||
| chr4:107989663-107989958 | Common:11; Rare:236; Clinvar:8; Clinvar (benign):10 | ||||
| chr4:108620347-108620709 | Common:12; Rare:308 | ||||
| chr4:108650269-108650725 | Common:4; Rare:273 | ||||
| chr4:109433370-109433700 | Common:1; Rare:88 | ||||
| chr4:109433723-109433890 | Common:2; Rare:118 | ||||
| chr4:109560026-109560372 | Common:10; Rare:210 | ||||
| chr4:109703391-109703587 | Common:1; Rare:67 | ||||
| chr4:109801935-109802249 | Common:1; Rare:53; Clinvar (benign):1 | ||||
| chr4:109815379-109815824 | Common:3; Rare:166 | ||||
| chr4:110198412-110198797 | Common:1; Rare:168 | ||||
| chr4:112231494-112231909 | Common:4; Rare:232 | ||||
| chr4:112232088-112232390 | Common:1; Rare:156 | ||||
| chr4:112285755-112285968 | Rare:100 | ||||
| chr4:112636858-112637202 | Common:2; Rare:182 |