Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:40425975-40426147 | Common:1; Rare:53 | ||||
chr19:40444271-40444490 | Common:3; Rare:71 | ||||
chr19:40465666-40466043 | Common:2; Rare:123 | ||||
chr19:40601217-40601384 | Rare:53 | ||||
chr19:40613824-40614038 | Common:1; Rare:69; Clinvar:2; Clinvar (benign):2 | ||||
chr19:40716875-40717009 | Common:1; Rare:44 | ||||
chr19:40750426-40750735 | Common:5; Rare:85 | ||||
chr19:41218697-41218994 | Common:8; Rare:63 | ||||
chr19:41310138-41310295 | Rare:69 | ||||
chr19:41397332-41397561 | Common:4; Rare:56 | ||||
chr19:41993114-41993306 | Rare:33 | ||||
chr19:42075862-42076191 | Rare:88 | ||||
chr19:42217671-42217881 | Rare:80 | ||||
chr19:42220120-42220349 | Common:2; Rare:64 | ||||
chr19:43504101-43504387 | Common:7; Rare:87 |