| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:36876642-36876889 | Common:1; Rare:73; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:37248846-37249036 | Common:2; Rare:35 | ||||
| chr5:37371040-37371198 | Rare:56 | ||||
| chr5:37379059-37379507 | Common:3; Rare:127 | ||||
| chr5:38557246-38557384 | Rare:37 | ||||
| chr5:38845712-38845810 | Common:1; Rare:26 | ||||
| chr5:39074373-39074522 | Common:1; Rare:67 | ||||
| chr5:40679703-40679971 | Common:1; Rare:61 | ||||
| chr5:40755826-40756060 | Rare:57 | ||||
| chr5:40798144-40798349 | Rare:80 | ||||
| chr5:40835184-40835314 | Common:2; Rare:58 | ||||
| chr5:40835333-40835423 | Rare:32 | ||||
| chr5:41870364-41870893 | Common:3; Rare:151; Clinvar:3; Clinvar (benign):3 | ||||
| chr5:43064833-43065143 | Common:1; Rare:73 | ||||
| chr5:43067348-43067500 | Rare:21 |