chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
91704146917041470AG7GENIChomozygous117681914
91704170217041703CT24GENIChomozygous117270068
91704271817042719TA25GENIChomozygous117768212
91704301217043013CT32GENIChomozygous117768214
91704309617043097TC43GENIChomozygous117768216
91704336417043365GA25GENIChomozygous117768218
91704363517043636GA20GENIChomozygous117768220
91704381817043819TA23GENIChomozygous117768222
91704470717044708GA13GENIChomozygous117768224
91704499217044993CT7GENIChomozygous117768226
91704579217045793AG11GENIChomozygous117768228
91704673217046733AG13GENIChomozygous117270069
91704805317048054GA27GENIChomozygous117681922
91704864617048647TA18GENIChomozygous117270071
91704869417048695TA29GENIChomozygous117270072
91704913817049139GC8GENIChomozygous117681924
91704932817049329GA20GENIChomozygous117681926
91704956117049562GA15GENIChomozygous117768230
91705015717050158GC14GENIChomozygous117768232
91705073517050736TC17GENIChomozygous117270073
91705234517052346TC13GENIChomozygous117768234
91705235317052354TC13GENIChomozygous117270077
91705270117052702CT15GENIChomozygous117768236
91705463717054638GA28GENIChomozygous117768238
91705792217057923CG8GENIChomozygous117270081
91705799717057998CG10GENIChomozygous117768240
91705869317058694TC10GENIChomozygous117681954
91705898617058987AG6GENIChomozygous117270083
91706038717060388GA12GENIChomozygous117681956