Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:73950117-73950330 | Common:5; Rare:85; Clinvar (benign):3 | ||||
chr14:74019262-74019427 | Common:1; Rare:64 | ||||
chr14:74493199-74493822 | Common:4; Rare:210; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
chr14:74713078-74713207 | Rare:63 | ||||
chr14:75127008-75127131 | Rare:42 | ||||
chr14:75427881-75428226 | Rare:82 | ||||
chr14:75660862-75661351 | Common:5; Rare:114 | ||||
chr14:77320817-77321097 | Rare:90; Clinvar:3 | ||||
chr14:77377055-77377410 | Common:2; Rare:102 | ||||
chr14:77457542-77457876 | Common:1; Rare:99 | ||||
chr14:77457987-77458103 | Rare:28 | ||||
chr14:77707988-77708109 | Rare:60 | ||||
chr14:85530055-85530180 | Common:1; Rare:30 | ||||
chr14:87993142-87993466 | Common:2; Rare:121; Clinvar:8; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
chr14:92121667-92121987 | Common:4; Rare:105 |