| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:169612258-169612441 | Rare:47; Clinvar:1 | ||||
| chr4:169612521-169612646 | Common:5; Rare:52; Clinvar:5; Clinvar (benign):2 | ||||
| chr4:169620358-169620956 | Common:2; Rare:170 | ||||
| chr4:169660030-169660095 | Common:1; Rare:9 | ||||
| chr4:169660111-169660412 | Rare:56 | ||||
| chr4:169679791-169680167 | Common:5; Rare:81 | ||||
| chr4:169757869-169758093 | Rare:64 | ||||
| chr4:170003730-170003881 | Rare:31 | ||||
| chr4:170026325-170026627 | Common:4; Rare:121 | ||||
| chr4:170027288-170027356 | Common:1; Rare:26 | ||||
| chr4:170089946-170090294 | Common:4; Rare:113 | ||||
| chr4:170091685-170091735 | Rare:11 | ||||
| chr4:170092004-170092168 | Common:2; Rare:42 | ||||
| chr4:173168200-173168254 | Rare:13 | ||||
| chr4:173168708-173168909 | Common:3; Rare:74 |