| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:81971779-81972059 | Common:3; Rare:111 | ||||
| chr5:82278319-82278692 | Common:4; Rare:121 | ||||
| chr5:83077339-83077615 | Common:1; Rare:79 | ||||
| chr5:84384378-84384737 | Rare:134 | ||||
| chr5:87267685-87267890 | Common:1; Rare:81 | ||||
| chr5:87268598-87268914 | Common:1; Rare:145; Clinvar:5; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr5:87412793-87413131 | Common:4; Rare:110 | ||||
| chr5:88827125-88827512 | Rare:63 | ||||
| chr5:88883026-88883373 | Rare:84; Clinvar:5; Clinvar (benign):2 | ||||
| chr5:88884521-88884761 | Common:1; Rare:46 | ||||
| chr5:88889294-88889350 | Rare:12 | ||||
| chr5:88889363-88889463 | Common:2; Rare:38 | ||||
| chr5:90409711-90410024 | Common:6; Rare:102 | ||||
| chr5:90474649-90474894 | Common:2; Rare:89 | ||||
| chr5:90529506-90529819 | Common:1; Rare:122 |