Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:41397558-41397853 | Common:7; Rare:104; Clinvar (benign):5 | ||||
chr19:41439496-41439686 | Common:1; Rare:55 | ||||
chr19:41860092-41860270 | Common:1; Rare:72; Clinvar:2; Clinvar (benign):1 | ||||
chr19:41959282-41959466 | Common:1; Rare:59 | ||||
chr19:41985039-41985374 | Common:1; Rare:83; Clinvar:4; Clinvar (benign):4 | ||||
chr19:41992991-41993294 | Rare:47 | ||||
chr19:41994072-41994585 | Common:1; Rare:115; Clinvar:2; Clinvar (benign):1 | ||||
chr19:42066130-42066335 | Common:1; Rare:37 | ||||
chr19:42069278-42069721 | Rare:102 | ||||
chr19:42070101-42070503 | Rare:96 | ||||
chr19:42075718-42076286 | Common:5; Rare:164 | ||||
chr19:42095903-42096194 | Rare:72 | ||||
chr19:42176028-42176083 | Common:4; Rare:12 | ||||
chr19:42217671-42217881 | Rare:80 | ||||
chr19:42220105-42220419 | Common:2; Rare:77 |