Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:40750434-40750885 | Common:6; Rare:113 | ||||
chr19:40777934-40778280 | Common:1; Rare:97 | ||||
chr19:41218726-41218992 | Common:7; Rare:57 | ||||
chr19:41310113-41310328 | Rare:89 | ||||
chr19:41397310-41397453 | Common:4; Rare:51 | ||||
chr19:41397487-41397853 | Common:8; Rare:117; Clinvar (benign):5 | ||||
chr19:42075817-42076168 | Rare:91 | ||||
chr19:42220117-42220349 | Common:2; Rare:64 | ||||
chr19:43575496-43575817 | Common:2; Rare:81 | ||||
chr19:43596132-43596433 | Common:2; Rare:95 | ||||
chr19:43619571-43619726 | Common:2; Rare:47 | ||||
chr19:43901795-43901911 | Common:2; Rare:24 | ||||
chr19:44072047-44072161 | Common:1; Rare:30 | ||||
chr19:44094251-44094410 | Common:1; Rare:31 | ||||
chr19:44141472-44141631 | Common:2; Rare:22 |