| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:168480458-168480521 | Rare:13 | ||||
| chr4:168831901-168832122 | Common:3; Rare:60 | ||||
| chr4:169010227-169010332 | Common:1; Rare:40 | ||||
| chr4:169270901-169271123 | Common:2; Rare:72 | ||||
| chr4:169620373-169620697 | Common:2; Rare:115 | ||||
| chr4:169660106-169660282 | Rare:34 | ||||
| chr4:169757873-169757966 | Rare:32 | ||||
| chr4:170089287-170089485 | Common:1; Rare:49 | ||||
| chr4:170089946-170090095 | Common:3; Rare:52 | ||||
| chr4:173369796-173369874 | Rare:25 | ||||
| chr4:173370690-173370967 | Common:2; Rare:70 | ||||
| chr4:173530205-173530353 | Rare:31 | ||||
| chr4:174283625-174283965 | Common:1; Rare:65 | ||||
| chr4:174522437-174522621 | Rare:60; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr4:176319794-176320055 | Common:3; Rare:99 |