| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:106315999-106316676 | Common:5; Rare:199 | ||||
| chr4:107720176-107720511 | Common:7; Rare:134 | ||||
| chr4:107824497-107824745 | Common:1; Rare:53 | ||||
| chr4:107824786-107825044 | Common:1; Rare:76 | ||||
| chr4:107989663-107989948 | Common:6; Rare:122; Clinvar:4; Clinvar (benign):5 | ||||
| chr4:108620357-108620711 | Common:6; Rare:160 | ||||
| chr4:108762874-108763178 | Common:1; Rare:86 | ||||
| chr4:109433779-109433815 | Rare:13 | ||||
| chr4:109703391-109703608 | Common:1; Rare:70 | ||||
| chr4:109729631-109730249 | Common:4; Rare:201 | ||||
| chr4:109801915-109802251 | Common:1; Rare:58; Clinvar (benign):1 | ||||
| chr4:109815380-109815803 | Common:2; Rare:109 | ||||
| chr4:110198500-110198885 | Rare:106 | ||||
| chr4:112145293-112145478 | Common:1; Rare:48 | ||||
| chr4:112231580-112231852 | Common:2; Rare:86 |