Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:54189374-54189429 | Rare:17 | ||||
chr19:54200745-54200898 | Common:3; Rare:64 | ||||
chr19:54222951-54223141 | Common:5; Rare:38 | ||||
chr19:54257204-54257367 | Common:1; Rare:36 | ||||
chr19:54449022-54449306 | Common:4; Rare:85 | ||||
chr19:54473199-54473380 | Rare:38 | ||||
chr19:55075587-55075924 | Common:3; Rare:85 | ||||
chr19:55094400-55094728 | Rare:106 | ||||
chr19:55156199-55156654 | Common:4; Rare:150; Clinvar:16; Clinvar (benign):12; Clinvar (pathogenic):1 | ||||
chr19:55157275-55157801 | Common:7; Rare:142; Clinvar:6; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr19:55207237-55207356 | Common:1; Rare:43 | ||||
chr19:55385751-55385961 | Common:5; Rare:71 | ||||
chr19:55461567-55461684 | Common:2; Rare:36 | ||||
chr19:55546035-55546388 | Common:1; Rare:70 | ||||
chr19:55599469-55599725 | Common:2; Rare:77 |