| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:169612547-169612783 | Common:5; Rare:79; Clinvar:3; Clinvar (benign):2 | ||||
| chr4:169620350-169620782 | Common:2; Rare:141 | ||||
| chr4:169660036-169660288 | Common:1; Rare:46 | ||||
| chr4:169757820-169758073 | Common:2; Rare:82 | ||||
| chr4:170026293-170026622 | Common:4; Rare:129 | ||||
| chr4:170027273-170027463 | Common:1; Rare:53 | ||||
| chr4:170089884-170090254 | Common:4; Rare:113 | ||||
| chr4:173168686-173168877 | Common:3; Rare:70 | ||||
| chr4:173333495-173333861 | Common:2; Rare:95 | ||||
| chr4:173334223-173334788 | Rare:142 | ||||
| chr4:173369732-173369953 | Common:1; Rare:71 | ||||
| chr4:173370681-173370976 | Common:2; Rare:76 | ||||
| chr4:174283255-174283353 | Rare:12 | ||||
| chr4:174283616-174284042 | Common:1; Rare:94 | ||||
| chr4:174284262-174284349 | Common:1; Rare:20 |