| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:164977591-164977964 | Common:1; Rare:89 | ||||
| chr4:165327411-165327741 | Common:2; Rare:95 | ||||
| chr4:168898312-168898580 | Common:1; Rare:66; Clinvar:6 | ||||
| chr4:169010233-169010434 | Common:1; Rare:59 | ||||
| chr4:169612266-169612441 | Rare:43; Clinvar:1 | ||||
| chr4:169612504-169612783 | Common:6; Rare:94; Clinvar:5; Clinvar (benign):2 | ||||
| chr4:169620373-169620702 | Common:2; Rare:115 | ||||
| chr4:169660127-169660272 | Rare:24 | ||||
| chr4:169757851-169758036 | Rare:58 | ||||
| chr4:170026287-170026583 | Common:4; Rare:109 | ||||
| chr4:173369605-173369935 | Common:2; Rare:79 | ||||
| chr4:173370672-173371019 | Common:2; Rare:88 | ||||
| chr4:173371164-173371391 | Common:3; Rare:78 | ||||
| chr4:173399233-173399476 | Common:3; Rare:31 | ||||
| chr4:173530205-173530334 | Rare:28 |