Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:69191421-69191572 | Rare:32 | ||||
chr14:69398256-69398381 | Rare:51 | ||||
chr14:69398595-69398731 | Rare:33 | ||||
chr14:71320253-71320491 | Rare:74 | ||||
chr14:73058337-73058612 | Common:3; Rare:89 | ||||
chr14:73458526-73458853 | Common:5; Rare:84 | ||||
chr14:73787175-73787372 | Common:2; Rare:74 | ||||
chr14:73950056-73950322 | Common:6; Rare:112; Clinvar (benign):4 | ||||
chr14:74019263-74019467 | Common:1; Rare:76 | ||||
chr14:74493215-74493777 | Common:4; Rare:183; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
chr14:74713100-74713208 | Rare:52 | ||||
chr14:75127001-75127122 | Rare:39 | ||||
chr14:75278946-75279114 | Rare:53 | ||||
chr14:75279524-75279657 | Rare:28 | ||||
chr14:75660797-75661346 | Common:4; Rare:132 |