| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:48016513-48016860 | Common:2; Rare:107 | ||||
| chr4:48269773-48270030 | Common:2; Rare:64 | ||||
| chr4:48341214-48341581 | Common:2; Rare:153 | ||||
| chr4:48520870-48520983 | Rare:12 | ||||
| chr4:48680933-48681069 | Common:1; Rare:29 | ||||
| chr4:48681076-48681249 | Common:1; Rare:33 | ||||
| chr4:48780156-48780572 | Common:3; Rare:127 | ||||
| chr4:48986115-48986313 | Rare:56 | ||||
| chr4:52659230-52659422 | Common:1; Rare:64 | ||||
| chr4:53365953-53366202 | Rare:56 | ||||
| chr4:53591438-53591642 | Common:2; Rare:42 | ||||
| chr4:54228937-54229363 | Common:1; Rare:88; Clinvar (benign):4 | ||||
| chr4:55346162-55346332 | Common:3; Rare:56; Clinvar:3; Clinvar (benign):2 | ||||
| chr4:55546816-55547012 | Common:2; Rare:68 | ||||
| chr4:56387417-56387547 | Rare:44 |