Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr18:74291884-74292272 | Common:4; Rare:114 | ||||
chr18:74496021-74496424 | Common:4; Rare:132 | ||||
chr18:74597601-74597889 | Common:2; Rare:77 | ||||
chr18:79988400-79988667 | Common:4; Rare:100; Clinvar (pathogenic):2 | ||||
chr19:572237-572618 | Common:3; Rare:186 | ||||
chr19:663138-663426 | Common:2; Rare:112 | ||||
chr19:893167-893484 | Common:3; Rare:132 | ||||
chr19:984228-984348 | Common:1; Rare:43 | ||||
chr19:1026471-1026680 | Common:1; Rare:81 | ||||
chr19:1132191-1132525 | Common:1; Rare:122 | ||||
chr19:2328565-2328703 | Common:2; Rare:70 | ||||
chr19:2900644-2900934 | Common:10; Rare:108 | ||||
chr19:3982805-3983221 | Common:5; Rare:146; Clinvar:1; Clinvar (benign):3 | ||||
chr19:4182532-4182692 | Common:1; Rare:58 | ||||
chr19:4723755-4724067 | Common:6; Rare:119 |