chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2235816340235816341GT16GENIChomozygous110839152
2235817405235817406GA18GENIChomozygous110839153
2235817617235817618TC20GENIChomozygous110317467
2235816499235816500TC15GENIChomozygous110317461
2235817289235817290TC15GENIChomozygous110317465
2235818503235818504GA25GENIChomozygous110839154
2235818679235818680TC22GENIChomozygous110317471
2235818795235818796GA29GENIChomozygous110839155
2235819016235819017GA14GENIChomozygous110317473
2235821717235821718AT11GENIChomozygous110839156
2235822251235822252AG15GENIChomozygous110839158
2235822382235822383AG16GENIChomozygous110317489
2235822876235822877TC8GENIChomozygous110317493
2235823695235823696GA16GENIChomozygous110317498
2235826991235826992AC28GENIChomozygous110839159
2235827217235827218AT21GENIChomozygous110839160
2235828145235828146TC2GENIChomozygous120180092
2235828146235828147CT3GENIChomozygous120180093
2235828152235828153AC5GENIChomozygous120180094
2235828162235828163AT5GENIChomozygous110912852
2235828982235828983AG20GENIChomozygous110839161
2235829428235829429AT27GENIChomozygous110839162
2235829721235829722CT15GENICpossibly homozygous110839163
2235829801235829802GA11GENIChomozygous110839164
2235830926235830927GT18GENIChomozygous110839166
2235830997235830998TC12GENIChomozygous110839167
2235831084235831085CT15GENIChomozygous110839168
2235831370235831371GC6GENIChomozygous110839169
2235831584235831585CT5GENIChomozygous110839170