| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:105710138-105710538 | Common:4; Rare:74 | ||||
| chr4:106315666-106316066 | Common:5; Rare:177 | ||||
| chr4:106316001-106316730 | Common:34; Rare:1027 | ||||
| chr4:107720174-107720715 | Common:43; Rare:1028 | ||||
| chr4:107931160-107931680 | Common:13; Rare:371; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr4:107988910-107989493 | Common:2; Rare:206 | ||||
| chr4:107989580-107990041 | Common:40; Rare:879; Clinvar:26; Clinvar (benign):33 | ||||
| chr4:108166444-108168079 | Common:20; Rare:1373; Clinvar (pathogenic):3 | ||||
| chr4:108168210-108168640 | Rare:104 | ||||
| chr4:108168609-108169048 | Common:8; Rare:297 | ||||
| chr4:108620254-108620713 | Common:44; Rare:1038 | ||||
| chr4:108621343-108622080 | Common:7; Rare:315 | ||||
| chr4:108650201-108650805 | Common:10; Rare:692 | ||||
| chr4:109433335-109433945 | Common:11; Rare:787 | ||||
| chr4:109433851-109434251 | Common:1; Rare:104 |