Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:27450522-27450685 | Common:2; Rare:63 | ||||
chr13:28139205-28139618 | Common:1; Rare:101 | ||||
chr13:28659062-28659210 | Common:1; Rare:63; Clinvar (pathogenic):1 | ||||
chr13:30306839-30307174 | Common:5; Rare:88 | ||||
chr13:30464314-30464574 | Common:2; Rare:80 | ||||
chr13:30465878-30466108 | Rare:71 | ||||
chr13:30617653-30617989 | Common:1; Rare:109 | ||||
chr13:32031308-32031353 | Rare:17 | ||||
chr13:32031638-32031783 | Common:1; Rare:46 | ||||
chr13:36297768-36297904 | Common:1; Rare:49 | ||||
chr13:36346287-36346530 | Common:3; Rare:67; Clinvar:3; Clinvar (benign):2 | ||||
chr13:36999301-36999457 | Rare:60 | ||||
chr13:37000352-37000407 | Rare:8 | ||||
chr13:37000501-37000821 | Common:3; Rare:101; Clinvar (pathogenic):1 | ||||
chr13:37059570-37059728 | Common:1; Rare:56 |