| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:53109719-53109877 | Common:1; Rare:83; Clinvar:3 | ||||
| chr5:55307639-55308023 | Common:4; Rare:128 | ||||
| chr5:57173548-57173925 | Common:2; Rare:135 | ||||
| chr5:60944968-60945399 | Common:6; Rare:174; Clinvar:7; Clinvar (benign):8; Clinvar (pathogenic):3 | ||||
| chr5:61162243-61162617 | Common:1; Rare:93 | ||||
| chr5:62403846-62404036 | Common:3; Rare:64 | ||||
| chr5:64768531-64768970 | Common:5; Rare:119 | ||||
| chr5:65563104-65563354 | Common:4; Rare:100 | ||||
| chr5:65624982-65625028 | Rare:12 | ||||
| chr5:65722013-65722273 | Common:2; Rare:91 | ||||
| chr5:65926482-65926718 | Common:5; Rare:69 | ||||
| chr5:69166927-69167163 | Common:1; Rare:54 | ||||
| chr5:69189446-69189630 | Common:1; Rare:59 | ||||
| chr5:69332747-69332870 | Rare:34 | ||||
| chr5:69369448-69369838 | Common:1; Rare:165 |