| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:35617818-35617989 | Rare:47 | ||||
| chr5:35938623-35938842 | Rare:39 | ||||
| chr5:35991588-35991743 | Rare:21 | ||||
| chr5:36000995-36001148 | Rare:30 | ||||
| chr5:36151828-36152174 | Rare:97 | ||||
| chr5:36241527-36241821 | Common:3; Rare:93; Clinvar:1; Clinvar (benign):5 | ||||
| chr5:36242135-36242338 | Common:1; Rare:53 | ||||
| chr5:36876650-36876907 | Common:1; Rare:78; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:36877064-36877310 | Rare:101; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:37249317-37249662 | Common:1; Rare:119; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:37303335-37303475 | Rare:32 | ||||
| chr5:37371011-37371540 | Common:3; Rare:145 | ||||
| chr5:37379193-37379547 | Rare:112 | ||||
| chr5:38258637-38258669 | Rare:11 | ||||
| chr5:38403413-38403567 | Rare:27 |