Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:77616578-77616743 | Common:2; Rare:61; Clinvar:3; Clinvar (benign):3 | ||||
chr14:77707979-77708207 | Common:2; Rare:118 | ||||
chr14:81220715-81221097 | Common:3; Rare:153 | ||||
chr14:81221275-81221347 | Rare:9 | ||||
chr14:81221360-81221450 | Common:1; Rare:29 | ||||
chr14:88562915-88563129 | Rare:102 | ||||
chr14:88824354-88824710 | Common:2; Rare:98; Clinvar:2; Clinvar (benign):1 | ||||
chr14:89954646-89954968 | Rare:100 | ||||
chr14:90331918-90332181 | Common:1; Rare:71 | ||||
chr14:90396882-90397142 | Common:2; Rare:130 | ||||
chr14:91510259-91510442 | Rare:60 | ||||
chr14:91510458-91510631 | Common:1; Rare:50 | ||||
chr14:92040026-92040177 | Common:2; Rare:42; Clinvar (benign):1 | ||||
chr14:92121650-92122005 | Common:5; Rare:123 | ||||
chr14:92793982-92794432 | Rare:142 |