Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:16542392-16542593 | Common:2; Rare:57 | ||||
chr19:16572373-16572679 | Common:5; Rare:118 | ||||
chr19:16660102-16660389 | Common:3; Rare:106 | ||||
chr19:17075405-17075760 | Common:5; Rare:143 | ||||
chr19:17226309-17226615 | Common:7; Rare:92 | ||||
chr19:17405583-17405684 | Common:1; Rare:20 | ||||
chr19:17511540-17511694 | Common:2; Rare:76 | ||||
chr19:18557674-18557905 | Common:5; Rare:58 | ||||
chr19:18919335-18919756 | Common:2; Rare:154 | ||||
chr19:19033448-19033649 | Common:2; Rare:68 | ||||
chr19:19033805-19033916 | Common:1; Rare:30 | ||||
chr19:19192107-19192273 | Common:1; Rare:50 | ||||
chr19:19192614-19193003 | Common:3; Rare:90; Clinvar (benign):1 | ||||
chr19:19320480-19320853 | Common:4; Rare:134 | ||||
chr19:19516155-19516258 | Rare:54; Clinvar (pathogenic):1 |