| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:102868806-102869068 | Common:2; Rare:87 | ||||
| chr4:103076270-103076394 | Rare:40 | ||||
| chr4:105399924-105400027 | Common:1; Rare:17 | ||||
| chr4:105708636-105708870 | Common:2; Rare:77 | ||||
| chr4:106316182-106316613 | Common:5; Rare:139 | ||||
| chr4:107720188-107720490 | Common:7; Rare:121 | ||||
| chr4:107989669-107989928 | Common:6; Rare:118; Clinvar:4; Clinvar (benign):5 | ||||
| chr4:108620391-108620739 | Common:6; Rare:149 | ||||
| chr4:108650268-108650667 | Common:2; Rare:128 | ||||
| chr4:109433757-109433836 | Common:1; Rare:30 | ||||
| chr4:109560082-109560396 | Common:5; Rare:90 | ||||
| chr4:109730063-109730242 | Common:2; Rare:44 | ||||
| chr4:109815379-109815798 | Common:2; Rare:108 | ||||
| chr4:110198535-110198854 | Rare:92 | ||||
| chr4:112231467-112231852 | Common:2; Rare:122 |