| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:34915218-34915371 | Rare:44 | ||||
| chr5:34915472-34915775 | Common:1; Rare:87 | ||||
| chr5:36151881-36152199 | Rare:100 | ||||
| chr5:36876639-36876850 | Common:1; Rare:63; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:38845717-38846078 | Common:2; Rare:93 | ||||
| chr5:40835189-40835398 | Common:1; Rare:83 | ||||
| chr5:43603102-43603250 | Rare:35 | ||||
| chr5:44808734-44808985 | Common:2; Rare:91 | ||||
| chr5:50667755-50667913 | Common:1; Rare:50 | ||||
| chr5:53109739-53109894 | Common:1; Rare:74; Clinvar:2 | ||||
| chr5:55307617-55308010 | Common:4; Rare:131 | ||||
| chr5:55534659-55534842 | Common:3; Rare:58 | ||||
| chr5:57173551-57173898 | Common:2; Rare:127 | ||||
| chr5:60945012-60945402 | Common:6; Rare:157; Clinvar:6; Clinvar (benign):8; Clinvar (pathogenic):2 | ||||
| chr5:61162268-61162628 | Common:1; Rare:89 |