Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:46387178-46387397 | Rare:60 | ||||
chr13:46797671-46797862 | Common:1; Rare:36 | ||||
chr13:48001238-48001384 | Common:1; Rare:69; Clinvar:3; Clinvar (benign):4 | ||||
chr13:48037488-48037789 | Common:1; Rare:120 | ||||
chr13:48037918-48038116 | Common:5; Rare:61 | ||||
chr13:48233059-48233475 | Common:3; Rare:144 | ||||
chr13:48303674-48304011 | Common:1; Rare:115; Clinvar:12; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
chr13:48533050-48533370 | Common:2; Rare:87 | ||||
chr13:48975668-48975934 | Common:2; Rare:82 | ||||
chr13:48976144-48976260 | Rare:33 | ||||
chr13:48976544-48976828 | Common:1; Rare:82 | ||||
chr13:49247823-49247982 | Rare:50 | ||||
chr13:49443997-49444528 | Common:2; Rare:167 | ||||
chr13:49585499-49585612 | Common:1; Rare:37 | ||||
chr13:49936240-49936592 | Common:1; Rare:107 |