| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:36242130-36242335 | Common:1; Rare:56 | ||||
| chr5:36301875-36302051 | Common:1; Rare:25 | ||||
| chr5:36876607-36877007 | Common:1; Rare:113; Clinvar:2; Clinvar (benign):3 | ||||
| chr5:37249285-37249433 | Common:1; Rare:49; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:37371001-37371197 | Rare:74 | ||||
| chr5:39074309-39074498 | Common:1; Rare:88 | ||||
| chr5:40679677-40679938 | Common:2; Rare:60 | ||||
| chr5:40755786-40756018 | Rare:50 | ||||
| chr5:40798101-40798438 | Common:1; Rare:128 | ||||
| chr5:40835165-40835316 | Common:2; Rare:67 | ||||
| chr5:41510726-41510810 | Common:1; Rare:14 | ||||
| chr5:41870360-41870535 | Rare:62; Clinvar:3 | ||||
| chr5:41903961-41904391 | Common:2; Rare:135 | ||||
| chr5:43064994-43065149 | Common:1; Rare:43 | ||||
| chr5:43067438-43067509 | Rare:11 |