chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
86490547064905471CG14GENIChomozygous126668223
86490551564905516CA30GENIChomozygous126668224
86490558064905581CA13GENIChomozygous126668225
86490559764905598CG12GENIChomozygous126668226
86492573064925731CT5GENICheterozygous126699126
86493781864937819TG11GENIChomozygous126668228
86494600464946005CT4GENIChomozygous126699127
86495914464959145AC10GENICheterozygous116518571
86496390664963907AG6GENICheterozygous116518573
86497821464978215GT17GENIChomozygous126668229
86498189764981898AC7GENIChomozygous117003635
86499842764998428TA4GENIChomozygous126668230
86502473065024731AT23GENIChomozygous126668231
86502704965027050CT18GENICheterozygous126668232
86502717565027176TC15GENICheterozygous116518591
86502725665027257TC12GENICheterozygous126692751
86506891765068918CG10GENIChomozygous116518595
86506892265068923AC10GENIChomozygous116518597
86506895965068960TA10GENIChomozygous116518599
86506896465068965GC11GENIChomozygous116518601
86506904965069050GC21GENIChomozygous116518603
86506915065069151TA9GENIChomozygous126668233
86521266565212666TG10GENICheterozygous117160839
86521277865212779GC19GENICheterozygous117044603
86525926265259263CA5GENICheterozygous126699128
86526300365263004CT5GENICheterozygous126699129
86526609765266098TG9GENICheterozygous126686032
86526912865269129CG9GENICheterozygous126692755
86527556365275564AG3GENICheterozygous126699130
86540517765405178CG3GENICheterozygous126699131