Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:73950050-73950323 | Common:6; Rare:114; Clinvar (benign):5 | ||||
chr14:74019252-74019429 | Common:1; Rare:69 | ||||
chr14:74493395-74493801 | Common:4; Rare:135; Clinvar (benign):4 | ||||
chr14:74502403-74502639 | Common:3; Rare:64 | ||||
chr14:74611488-74612057 | Rare:196; Clinvar:9; Clinvar (benign):1 | ||||
chr14:74612148-74612379 | Common:1; Rare:41; Clinvar:1; Clinvar (benign):1 | ||||
chr14:74612581-74612768 | Common:1; Rare:52 | ||||
chr14:74713052-74713205 | Rare:86 | ||||
chr14:74881781-74881959 | Common:1; Rare:77 | ||||
chr14:75126865-75127120 | Rare:81 | ||||
chr14:75578492-75578685 | Common:2; Rare:37; Clinvar (benign):1 | ||||
chr14:75660825-75661304 | Common:4; Rare:114 | ||||
chr14:75982974-75983251 | Common:3; Rare:48 | ||||
chr14:76762516-76762839 | Rare:84 | ||||
chr14:77377053-77377410 | Common:2; Rare:104 |