Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:19033831-19033916 | Common:1; Rare:21 | ||||
chr19:19192115-19192264 | Common:1; Rare:48 | ||||
chr19:19203404-19203433 | Rare:12 | ||||
chr19:19320472-19320850 | Common:4; Rare:140 | ||||
chr19:19516126-19516296 | Rare:115; Clinvar:1; Clinvar (pathogenic):1 | ||||
chr19:19821721-19821905 | Common:1; Rare:58 | ||||
chr19:20167022-20167243 | Common:2; Rare:83 | ||||
chr19:20565752-20565932 | Rare:49 | ||||
chr19:32971897-32972277 | Common:4; Rare:111 | ||||
chr19:33081074-33081223 | Common:2; Rare:53 | ||||
chr19:33521765-33521936 | Rare:53; Clinvar:3 | ||||
chr19:34172420-34172570 | Rare:64 | ||||
chr19:34254513-34254601 | Rare:24 | ||||
chr19:34428333-34428435 | Rare:45 | ||||
chr19:34677548-34677758 | Common:5; Rare:59 |