chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
91446956514469566G-2GENICheterozygous51763220
91447995814479960AC--2GENICheterozygous52944766
91448099214480993TTC18GENIChomozygous52337138
91448387514483876GC8GENIChomozygous51763265
91448833914488343GAGA----3GENICheterozygous52337139
91448978114489782CCTTT3GENICheterozygous52898807
91449160514491607GT--4GENICheterozygous52898811
91449382114493822TC12GENIChomozygous52337140
91449450514494506A-28GENIChomozygous52337141
91449450814494509CG29GENIChomozygous52898813
91449478414494785AG29GENIChomozygous51763307
91449483214494833AATG30GENIChomozygous52337142
91449493214494933TG33GENIChomozygous51763309
91449496414494965TC30GENIChomozygous52337143
91449502014495021AATG23GENIChomozygous52337144
91449643614496437CT4GENIChomozygous52337145
91449681614496817AG14GENIChomozygous51763313
91449754514497547GA--7GENIChomozygous52898817
91449754814497552ACAG----7GENIChomozygous52898819
91449807014498076GTGTGT------10GENICpossibly homozygous52898823
91449867914498680TA27GENIChomozygous52337148
91449917414499175CA20GENIChomozygous52337149
91449966114499662AG21GENIChomozygous51763321
91450037314500374CT6GENICheterozygous52898825
91450037714500378CT10GENIChomozygous52898827
91450037914500380CT10GENIChomozygous52898829
91450038114500382CT9GENIChomozygous52898831
91450038314500384CT8GENIChomozygous52898833
91450038514500386CT7GENIChomozygous52898835
91450192814501929AC21GENIChomozygous51763327