| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:1172791-1173127 | Common:5; Rare:52 | ||||
| chr4:1712179-1712451 | Common:4; Rare:115 | ||||
| chr4:1801324-1801713 | Common:5; Rare:145; Clinvar:3; Clinvar (benign):13 | ||||
| chr4:1804470-1804969 | Common:3; Rare:178; Clinvar:4; Clinvar (benign):8 | ||||
| chr4:1974369-1974635 | Common:1; Rare:58 | ||||
| chr4:2468957-2469178 | Common:2; Rare:78 | ||||
| chr4:2798682-2799147 | Common:5; Rare:95 | ||||
| chr4:2843745-2843996 | Common:3; Rare:85 | ||||
| chr4:2934767-2934940 | Common:4; Rare:78 | ||||
| chr4:2963322-2963587 | Common:2; Rare:96 | ||||
| chr4:3074619-3074754 | Common:2; Rare:54 | ||||
| chr4:3292718-3293060 | Common:3; Rare:134 | ||||
| chr4:3385433-3385586 | Common:2; Rare:33 | ||||
| chr4:3386109-3386363 | Common:1; Rare:41 | ||||
| chr4:3532211-3532455 | Rare:133; Clinvar (pathogenic):2 |