Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:41225665-41225793 | Rare:30 | ||||
chr19:41352986-41353352 | Common:4; Rare:90; Clinvar (benign):2 | ||||
chr19:41956424-41956736 | Common:2; Rare:62 | ||||
chr19:42396922-42397184 | Common:1; Rare:61 | ||||
chr19:44847586-44847976 | Common:2; Rare:89 | ||||
chr19:45442860-45443081 | Rare:40 | ||||
chr19:45444244-45444517 | Common:1; Rare:62 | ||||
chr19:45451533-45451654 | Rare:31 | ||||
chr19:45455768-45455982 | Common:1; Rare:51 | ||||
chr19:46133317-46133639 | Common:1; Rare:55 | ||||
chr19:46180860-46181099 | Rare:58 | ||||
chr19:46203081-46203190 | Common:2; Rare:17 | ||||
chr19:46860831-46861118 | Common:3; Rare:93 | ||||
chr19:47273242-47273362 | Rare:34 | ||||
chr19:48873021-48873331 | Common:4; Rare:64 |