Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:52369874-52369954 | Rare:26 | ||||
chr19:52397699-52397895 | Common:5; Rare:61 | ||||
chr19:52690451-52690749 | Common:6; Rare:70 | ||||
chr19:52735016-52735218 | Common:4; Rare:61 | ||||
chr19:52786726-52786939 | Common:8; Rare:59 | ||||
chr19:52962817-52963166 | Common:4; Rare:105 | ||||
chr19:53254786-53255067 | Common:4; Rare:101 | ||||
chr19:53554487-53554613 | Common:2; Rare:36 | ||||
chr19:53866319-53866399 | Common:2; Rare:17 | ||||
chr19:53867682-53867954 | Common:1; Rare:69 | ||||
chr19:53869300-53869633 | Common:2; Rare:90 | ||||
chr19:54102684-54102887 | Common:3; Rare:54 | ||||
chr19:54115289-54115591 | Common:2; Rare:68; Clinvar (benign):2 | ||||
chr19:54115628-54115797 | Common:1; Rare:43; Clinvar:4 | ||||
chr19:54159663-54160068 | Rare:138 |