| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:36066780-36067067 | Common:1; Rare:77 | ||||
| chr5:36151857-36152240 | Rare:116 | ||||
| chr5:36242049-36242270 | Common:2; Rare:55; Clinvar (benign):2 | ||||
| chr5:36606476-36606681 | Rare:34 | ||||
| chr5:36876650-36876910 | Common:1; Rare:78; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:37370987-37371305 | Common:1; Rare:98 | ||||
| chr5:37379156-37379351 | Common:1; Rare:45 | ||||
| chr5:37839902-37839916 | Rare:2 | ||||
| chr5:38556571-38556888 | Common:3; Rare:117 | ||||
| chr5:38845761-38846016 | Rare:64 | ||||
| chr5:39074388-39074522 | Common:1; Rare:59 | ||||
| chr5:40679705-40679932 | Common:1; Rare:48 | ||||
| chr5:40755774-40756064 | Rare:64 | ||||
| chr5:40798152-40798461 | Common:2; Rare:119 | ||||
| chr5:40835144-40835438 | Common:3; Rare:123 |