Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:25287224-25287639 | Common:3; Rare:132 | ||||
chr13:25301447-25301753 | Common:2; Rare:110 | ||||
chr13:25371837-25372218 | Rare:110 | ||||
chr13:25468597-25468975 | Common:1; Rare:126 | ||||
chr13:26221695-26222001 | Rare:88 | ||||
chr13:26222246-26222368 | Common:2; Rare:35 | ||||
chr13:26557466-26557794 | Common:4; Rare:131 | ||||
chr13:27251225-27251762 | Common:9; Rare:163 | ||||
chr13:27424460-27424740 | Common:5; Rare:95 | ||||
chr13:27449968-27450230 | Common:3; Rare:77 | ||||
chr13:27450529-27450627 | Common:2; Rare:44 | ||||
chr13:27620453-27620838 | Common:3; Rare:131 | ||||
chr13:28138087-28138229 | Common:1; Rare:49 | ||||
chr13:28658942-28659194 | Rare:107; Clinvar (pathogenic):1 | ||||
chr13:28718928-28719123 | Common:1; Rare:47 |