chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
31508936115089369ACACACAC--------43GENIChomozygous58571519
31508954715089551ACAG----37GENIChomozygous59662800
31509010715090108AG36GENIChomozygous58086188
31509116015091161TC78GENIChomozygous58086190
31509126415091265CA57GENICpossibly homozygous59999682
31509140815091409GA25GENIChomozygous59999683
31509184815091849AC53GENIChomozygous58086194
31509193115091932CT35GENIChomozygous59999684
31509204315092044TC24GENIChomozygous59999685
31509228815092289CT41GENIChomozygous59999686
31509229115092292GA40GENIChomozygous59999687
31509241515092416GA19GENIChomozygous59999688
31509261015092611GA34GENIChomozygous59999689
31509280115092802CG49GENICpossibly homozygous59999690
31509280515092806AATG48GENIChomozygous59999691
31509301715093018GA32GENIChomozygous59999692
31509353615093537CT28GENIChomozygous58086205
31509362615093627TC30GENIChomozygous58086207
31509371215093713TTAC31GENICpossibly homozygous58086211
31509382215093823AG34GENIChomozygous58086213
31509394515093946AG35GENIChomozygous58086215
31509401315094015TT--14GENIChomozygous58086217
31509419215094193GA54GENIChomozygous58086220
31509438915094390AG29GENIChomozygous58086222
31509463515094636AC40GENIChomozygous59999693
31509465615094657AAAAAC34GENIChomozygous58086224
31509488415094885TTGC8GENICheterozygous58571522
31509502715095028TA36GENIChomozygous58086230
31509523815095239CCT18GENIChomozygous58086232
31509550515095506TC57GENIChomozygous58086234
31509605715096058CT35GENIChomozygous59999694
31509620715096208CT56GENIChomozygous59999695
31509707715097078GA29GENICpossibly homozygous59999696
31509734015097341GA27GENIChomozygous59999697
31509735915097360GC24GENIChomozygous58086238
31509746715097468AG42GENIChomozygous58086242
31509805415098055GC57GENIChomozygous58277452