chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3117040660117040661GA23GENIChomozygous57619133
3117040898117040899AT21GENIChomozygous57619135
3117040915117040916TA18GENIChomozygous57619137
3117040918117040919GT20GENIChomozygous57619139
3117040927117040928GT17GENIChomozygous57619141
3117040934117040935CG16GENIChomozygous57619143
3117040941117040942TTTG14GENIChomozygous58620537
3117040944117040946CT--13GENIChomozygous58620538
3117040965117040966AC7GENIChomozygous57619145
3117041953117041954TTC10GENIChomozygous58620539
3117041982117041983GGT10GENIChomozygous57619167
3117044329117044330C-7GENIChomozygous57619169
3117045840117045841GA35GENICpossibly homozygous58178074
3117043799117043800C-18GENIChomozygous58178068
3117044375117044376TC21GENIChomozygous58178070
3117045634117045635AT27GENIChomozygous58178072
3117046378117046379TC27GENIChomozygous58009087
3117046621117046622CT20GENIChomozygous57619171
3117046737117046738TC14GENIChomozygous58009090
3117047987117047988GT24GENIChomozygous58178076
3117050638117050639GA19GENIChomozygous58009101
3117051087117051088AT18GENIChomozygous58009104
3117051484117051485GA23GENIChomozygous57619176
3117051702117051708ACACAC------8GENIChomozygous58620541
3117052758117052759AG21GENIChomozygous58009109
3117055777117055778GA31GENIChomozygous58178080
3117055825117055826GC38GENIChomozygous58009115
3117056117117056118GC25GENIChomozygous58009121
3117053965117053966CG22GENIChomozygous57619178
3117057521117057522CT30GENIChomozygous58178082
3117057850117057851TC21GENIChomozygous58009127