| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:2831621-2831912 | Common:3; Rare:99; Clinvar:3; Clinvar (benign):2 | ||||
| chr4:2939610-2939849 | Common:2; Rare:90 | ||||
| chr4:3041492-3041828 | Common:4; Rare:84 | ||||
| chr4:3225281-3225441 | Rare:33 | ||||
| chr4:3767153-3767222 | Rare:26 | ||||
| chr4:3767261-3767295 | Rare:9 | ||||
| chr4:3955417-3955643 | Common:8; Rare:68 | ||||
| chr4:6673165-6673447 | Common:3; Rare:65 | ||||
| chr4:6673837-6673934 | Common:5; Rare:51 | ||||
| chr4:6916726-6916912 | Common:1; Rare:46 | ||||
| chr4:6925441-6925817 | Common:4; Rare:82 | ||||
| chr4:7646753-7646974 | Common:1; Rare:47 | ||||
| chr4:10006239-10006484 | Common:2; Rare:45 | ||||
| chr4:15002028-15002065 | Rare:14 | ||||
| chr4:15005058-15005099 | Rare:19 |