Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:18571643-18571904 | Common:3; Rare:111 | ||||
chr19:18919328-18919763 | Common:3; Rare:167 | ||||
chr19:19033475-19033610 | Common:2; Rare:47 | ||||
chr19:19033820-19033914 | Common:1; Rare:25 | ||||
chr19:19192090-19192262 | Common:1; Rare:55 | ||||
chr19:19192590-19193015 | Common:3; Rare:105; Clinvar (benign):1 | ||||
chr19:19320480-19320848 | Common:4; Rare:131 | ||||
chr19:19516163-19516258 | Rare:48; Clinvar (pathogenic):1 | ||||
chr19:29213131-29213290 | Common:3; Rare:53 | ||||
chr19:29606207-29606315 | Rare:39 | ||||
chr19:32691787-32691924 | Common:5; Rare:38 | ||||
chr19:32692259-32692390 | Common:1; Rare:76 | ||||
chr19:32971964-32972274 | Common:3; Rare:86 | ||||
chr19:33081139-33081192 | Common:1; Rare:22 | ||||
chr19:33521762-33521956 | Common:1; Rare:58; Clinvar:4 |