| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:36151880-36152174 | Rare:91 | ||||
| chr5:36876625-36876889 | Common:1; Rare:78; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:37249325-37249486 | Common:1; Rare:62; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:38845715-38846080 | Common:2; Rare:96 | ||||
| chr5:39074350-39074530 | Common:1; Rare:83 | ||||
| chr5:39425010-39425308 | Common:2; Rare:65 | ||||
| chr5:40679301-40679385 | Rare:15 | ||||
| chr5:40679698-40679924 | Common:1; Rare:46 | ||||
| chr5:40798125-40798401 | Common:1; Rare:103 | ||||
| chr5:40835173-40835417 | Common:2; Rare:96 | ||||
| chr5:41870372-41870553 | Common:1; Rare:59; Clinvar:2; Clinvar (benign):1 | ||||
| chr5:41904003-41904377 | Common:2; Rare:115 | ||||
| chr5:43043215-43043313 | Common:1; Rare:21 | ||||
| chr5:43064823-43065137 | Rare:72 | ||||
| chr5:43067334-43067502 | Rare:24 |