Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:48393493-48393860 | Common:1; Rare:103 | ||||
chr19:48473930-48474193 | Common:2; Rare:82 | ||||
chr19:48644888-48645054 | Rare:25 | ||||
chr19:49829858-49830102 | Common:1; Rare:91; Clinvar:4; Clinvar (benign):4 | ||||
chr19:50718362-50718521 | Rare:38 | ||||
chr19:51354752-51354984 | Common:1; Rare:38 | ||||
chr19:51688480-51688664 | Common:3; Rare:34 | ||||
chr19:51949038-51949243 | Common:6; Rare:50 | ||||
chr19:52923440-52923511 | Common:2; Rare:29 | ||||
chr19:52993514-52993790 | Common:3; Rare:57 | ||||
chr19:55241030-55241251 | Common:1; Rare:76 | ||||
chr19:55694938-55695161 | Common:1; Rare:65 | ||||
chr19:56706595-56706706 | Common:1; Rare:12 | ||||
chr19:56765226-56765377 | Common:1; Rare:45 | ||||
chr19:56826460-56826692 | Common:1; Rare:40 |