Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:73950080-73950323 | Common:5; Rare:96; Clinvar (benign):3 | ||||
chr14:74019233-74019423 | Common:1; Rare:74 | ||||
chr14:74493568-74493767 | Common:3; Rare:75; Clinvar (benign):3 | ||||
chr14:74713074-74713200 | Rare:65 | ||||
chr14:74881795-74881982 | Common:1; Rare:88 | ||||
chr14:75002598-75002947 | Common:1; Rare:97; Clinvar:2 | ||||
chr14:75051428-75051530 | Common:2; Rare:28; Clinvar:3; Clinvar (benign):2 | ||||
chr14:75126985-75127106 | Rare:39 | ||||
chr14:75578337-75578697 | Common:2; Rare:69; Clinvar (benign):1 | ||||
chr14:75660821-75661043 | Rare:58 | ||||
chr14:75661162-75661315 | Common:2; Rare:42 | ||||
chr14:77320838-77321067 | Rare:68; Clinvar:1 | ||||
chr14:77377045-77377133 | Common:1; Rare:34 | ||||
chr14:77457536-77457876 | Common:1; Rare:103 | ||||
chr14:77708000-77708114 | Rare:54 |