| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:169010233-169010480 | Common:1; Rare:74 | ||||
| chr4:169612562-169612783 | Common:4; Rare:72; Clinvar:2; Clinvar (benign):2 | ||||
| chr4:169620358-169620707 | Common:2; Rare:124 | ||||
| chr4:169660033-169660316 | Common:1; Rare:52 | ||||
| chr4:169757869-169758117 | Rare:68 | ||||
| chr4:170026293-170026580 | Common:4; Rare:107 | ||||
| chr4:171813292-171813403 | Common:1; Rare:39 | ||||
| chr4:173334271-173334656 | Rare:104 | ||||
| chr4:173369778-173369935 | Common:1; Rare:51 | ||||
| chr4:173370690-173370986 | Common:2; Rare:76 | ||||
| chr4:174283549-174283965 | Common:1; Rare:80 | ||||
| chr4:174522464-174522587 | Rare:39; Clinvar:1 | ||||
| chr4:174829148-174829412 | Common:1; Rare:61 | ||||
| chr4:175812205-175812859 | Common:11; Rare:148 | ||||
| chr4:176002317-176002589 | Rare:81 |