| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:26860579-26860804 | Common:1; Rare:74 | ||||
| chr4:39458849-39459060 | Common:3; Rare:116 | ||||
| chr4:55395866-55396007 | Rare:44; Clinvar:2 | ||||
| chr4:56435554-56435744 | Common:3; Rare:64 | ||||
| chr4:56467565-56467699 | Common:2; Rare:57; Clinvar (benign):5 | ||||
| chr4:57110069-57110304 | Rare:75 | ||||
| chr4:67701136-67701365 | Common:4; Rare:102 | ||||
| chr4:73869528-73869548 | Rare:7 | ||||
| chr4:74038675-74038937 | Rare:68 | ||||
| chr4:75514288-75514485 | Rare:63 | ||||
| chr4:75724417-75724692 | Common:1; Rare:79 | ||||
| chr4:76148364-76148575 | Common:3; Rare:67 | ||||
| chr4:76949618-76949843 | Rare:63 | ||||
| chr4:78939368-78939509 | Rare:67 | ||||
| chr4:82429279-82429578 | Common:1; Rare:168; Clinvar:7; Clinvar (benign):6 |