Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:40777910-40778280 | Common:1; Rare:101 | ||||
chr19:41219047-41219403 | Common:1; Rare:86 | ||||
chr19:41262326-41262598 | Rare:49 | ||||
chr19:41860120-41860278 | Common:1; Rare:63; Clinvar:2; Clinvar (benign):1 | ||||
chr19:42075843-42076214 | Rare:102 | ||||
chr19:42220128-42220341 | Common:2; Rare:60 | ||||
chr19:43527173-43527315 | Common:4; Rare:57; Clinvar:3; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
chr19:43670163-43670286 | Common:1; Rare:24 | ||||
chr19:43754840-43755106 | Common:3; Rare:103 | ||||
chr19:44002776-44002993 | Common:5; Rare:55 | ||||
chr19:44094203-44094431 | Common:1; Rare:58 | ||||
chr19:44141476-44141649 | Common:2; Rare:24 | ||||
chr19:44356666-44356851 | Common:1; Rare:39 | ||||
chr19:44500505-44500625 | Common:1; Rare:31 | ||||
chr19:44643798-44643918 | Rare:36 |