| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:36241624-36241966 | Common:4; Rare:117; Clinvar:1; Clinvar (benign):4 | ||||
| chr5:36242126-36242334 | Common:1; Rare:57 | ||||
| chr5:36606470-36606671 | Rare:34 | ||||
| chr5:36876623-36876915 | Common:1; Rare:86; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:36876972-36877172 | Rare:62; Clinvar:2; Clinvar (benign):1 | ||||
| chr5:37249285-37249547 | Common:1; Rare:89; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:37371003-37371393 | Common:2; Rare:104 | ||||
| chr5:37379044-37379380 | Common:3; Rare:84 | ||||
| chr5:38845712-38846063 | Common:2; Rare:92 | ||||
| chr5:39074333-39074539 | Common:1; Rare:103 | ||||
| chr5:39219521-39219808 | Common:2; Rare:57 | ||||
| chr5:39424806-39424923 | Rare:44 | ||||
| chr5:39424929-39425428 | Common:4; Rare:104 | ||||
| chr5:39462068-39462560 | Common:1; Rare:90 | ||||
| chr5:40679298-40679445 | Common:1; Rare:30 |