| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:35617636-35617921 | Common:1; Rare:51 | ||||
| chr5:36151874-36152195 | Rare:102 | ||||
| chr5:36242135-36242334 | Common:1; Rare:52 | ||||
| chr5:36876623-36876938 | Common:1; Rare:91; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:37371040-37371382 | Common:2; Rare:84 | ||||
| chr5:37379168-37379364 | Common:1; Rare:49 | ||||
| chr5:38845722-38846080 | Common:2; Rare:93 | ||||
| chr5:39074327-39074549 | Common:1; Rare:112 | ||||
| chr5:39424929-39425307 | Common:3; Rare:78 | ||||
| chr5:40679177-40679409 | Common:3; Rare:48 | ||||
| chr5:40755891-40756050 | Rare:43 | ||||
| chr5:40798108-40798461 | Common:2; Rare:134 | ||||
| chr5:40834979-40835406 | Common:3; Rare:165 | ||||
| chr5:41925203-41925322 | Rare:43 | ||||
| chr5:43064823-43065147 | Common:1; Rare:74 |