| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:10250183-10250377 | Common:3; Rare:99; Clinvar:4; Clinvar (benign):2 | ||||
| chr5:10353622-10353903 | Common:3; Rare:100 | ||||
| chr5:31532040-31532362 | Common:3; Rare:94 | ||||
| chr5:32174252-32174416 | Common:1; Rare:61 | ||||
| chr5:33440802-33441075 | Common:4; Rare:73 | ||||
| chr5:34656121-34656508 | Common:3; Rare:100 | ||||
| chr5:34915497-34915845 | Common:2; Rare:100 | ||||
| chr5:36876650-36876874 | Common:1; Rare:67; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:40679697-40679960 | Common:1; Rare:59 | ||||
| chr5:40798137-40798302 | Rare:68 | ||||
| chr5:44808694-44809016 | Common:2; Rare:117 | ||||
| chr5:53109719-53109854 | Rare:74; Clinvar:3 | ||||
| chr5:55307617-55308010 | Common:4; Rare:131 | ||||
| chr5:60945006-60945238 | Common:5; Rare:96; Clinvar:4; Clinvar (benign):5 | ||||
| chr5:61162372-61162613 | Common:1; Rare:67 |