Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:44002809-44002988 | Common:4; Rare:44 | ||||
chr19:44025231-44025394 | Common:1; Rare:33 | ||||
chr19:44072020-44072173 | Common:1; Rare:38 | ||||
chr19:44094251-44094421 | Common:1; Rare:37 | ||||
chr19:44113120-44113453 | Common:5; Rare:76 | ||||
chr19:44141483-44141636 | Common:2; Rare:21 | ||||
chr19:44212363-44212575 | Common:4; Rare:65 | ||||
chr19:44305001-44305140 | Rare:36 | ||||
chr19:44356645-44356820 | Common:1; Rare:31 | ||||
chr19:44500508-44500602 | Common:1; Rare:23 | ||||
chr19:44643798-44643918 | Rare:36 | ||||
chr19:45370552-45370756 | Common:2; Rare:63 | ||||
chr19:45406341-45406649 | Common:1; Rare:67 | ||||
chr19:45423502-45423710 | Common:2; Rare:45; Clinvar (benign):1 | ||||
chr19:45467884-45468023 | Rare:44 |