Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:77376959-77377421 | Common:5; Rare:133 | ||||
chr14:77457542-77457877 | Common:1; Rare:99 | ||||
chr14:77457966-77458155 | Rare:54 | ||||
chr14:77616562-77617084 | Common:3; Rare:139; Clinvar:3; Clinvar (benign):5 | ||||
chr14:77707985-77708201 | Common:2; Rare:111 | ||||
chr14:80212109-80212358 | Common:2; Rare:39 | ||||
chr14:80955198-80955237 | Rare:7 | ||||
chr14:81220843-81221069 | Common:1; Rare:106 | ||||
chr14:81221269-81221423 | Common:1; Rare:34 | ||||
chr14:81436376-81436626 | Common:4; Rare:92 | ||||
chr14:85530024-85530190 | Common:1; Rare:36 | ||||
chr14:87993055-87993294 | Common:4; Rare:111; Clinvar:12; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
chr14:88005116-88005198 | Rare:12 | ||||
chr14:88473873-88474031 | Common:1; Rare:31 | ||||
chr14:88562926-88563163 | Rare:104 |