Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:73569136-73569292 | Rare:43 | ||||
chr14:73644885-73645041 | Common:2; Rare:43; Clinvar:2 | ||||
chr14:73787118-73787372 | Common:2; Rare:89 | ||||
chr14:73886782-73886893 | Common:2; Rare:36 | ||||
chr14:73950053-73950333 | Common:6; Rare:120; Clinvar (benign):4 | ||||
chr14:74019216-74019483 | Common:2; Rare:100 | ||||
chr14:74302899-74303026 | Rare:62; Clinvar (benign):3 | ||||
chr14:74493240-74493788 | Common:4; Rare:176; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr14:74611562-74611679 | Rare:39 | ||||
chr14:74612189-74612348 | Rare:33 | ||||
chr14:74713053-74713235 | Rare:99 | ||||
chr14:74881819-74881973 | Rare:69 | ||||
chr14:75069493-75069689 | Common:1; Rare:46 | ||||
chr14:75126950-75127123 | Rare:62 | ||||
chr14:75176353-75176538 | Rare:42 |