chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
171390701113907012TG1GENIChomozygous64290860
171390916913909170GT19GENIChomozygous64685216
171390919713909198AG12GENIChomozygous64290870
171391038013910381TG3GENIChomozygous64290878
171391061913910620AG8GENICpossibly homozygous64290880
171391062313910624TC9GENIChomozygous64290882
171391104613911047GA17GENIChomozygous64685218
171391122713911228GA14GENIChomozygous64685220
171391242113912422AG10GENIChomozygous64290886
171391293113912932TC6GENIChomozygous64290888
171391304313913044GA11GENIChomozygous64685224
171391317213913173CT9GENIChomozygous64685226
171391506713915068GA16GENIChomozygous64685228
171391580213915803TC6GENIChomozygous64290890
171391618213916183AT7GENIChomozygous64685230
171391694013916941CT10GENIChomozygous64685232
171391730813917309AG7GENIChomozygous64290898
171392017413920175TC13GENIChomozygous64290948
171392052213920523CT8GENIChomozygous64290956
171392060213920603TC8GENIChomozygous64290961
171392326113923262AC12GENIChomozygous64290995
171392349313923494GA8GENIChomozygous64291003
171392367213923673TC8GENIChomozygous64685234
171392519213925193CT8GENIChomozygous64685236
171392544813925449TC5GENIChomozygous64685238
171392559413925595CG14GENIChomozygous64685240
171392572513925726TC14GENIChomozygous64291035
171392551313925514GT11GENIChomozygous64291031
171392633413926335GA11GENIChomozygous64291051
171392711013927111TC4GENIChomozygous64291059
171392727613927277TC6GENIChomozygous64291061
171392729713927298TC10GENIChomozygous64291065
171392760713927608AG8GENIChomozygous64291076
171392788013927881CA12GENIChomozygous64685242
171392888513928886TC3GENIChomozygous64685244
171393022613930227CG10GENICheterozygous64291080
171393136413931365TC12GENIChomozygous64291082
171393164413931645CT8GENIChomozygous64291084
171393264813932649TC9GENIChomozygous64291086
171393274013932741AG10GENIChomozygous64291088
171393275313932754CT7GENIChomozygous64291090
171393301713933018TC9GENIChomozygous64291092