Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:5894541-5894738 | Common:2; Rare:65; Clinvar:3 | ||||
chr19:6682140-6682350 | Rare:53 | ||||
chr19:6707076-6707534 | Common:2; Rare:139; Clinvar:1; Clinvar (benign):4 | ||||
chr19:6709682-6710119 | Common:7; Rare:105; Clinvar:4; Clinvar (benign):2 | ||||
chr19:6718092-6718343 | Rare:64; Clinvar:2 | ||||
chr19:7197327-7197613 | Common:15; Rare:93 | ||||
chr19:7198044-7198313 | Common:5; Rare:88 | ||||
chr19:7228982-7229089 | Common:3; Rare:20 | ||||
chr19:7787371-7787524 | Common:1; Rare:21 | ||||
chr19:9407021-9407132 | Common:2; Rare:40 | ||||
chr19:11024286-11024356 | Rare:26; Clinvar (benign):4 | ||||
chr19:12194924-12195051 | Common:1; Rare:46 | ||||
chr19:12793554-12793749 | Common:3; Rare:49 | ||||
chr19:12796695-12796884 | Rare:43 | ||||
chr19:13104390-13104552 | Rare:38 |