chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
65851631158516312AC46GENICheterozygous541259334
65851688958516890TTC8GENIChomozygous697340835
65851736958517370TTG14GENIChomozygous697340836
65851826458518265T-22GENIChomozygous697340837
65851857358518574TTAA2GENIChomozygous697340838
65851858858518589C-5GENIChomozygous697340839
65851886958518870AT23GENICpossibly homozygous538487896
65851996258519963CT21GENIChomozygous538487897
65852014958520165TCTCTCTCTCTCTCTC----------------6GENIChomozygous697340840
65852020458520205CG19GENICheterozygous541259335
65852185958521860CCA9GENIChomozygous697340841
65852232058522321CG38GENIChomozygous538487898
65852352258523523CT33GENIChomozygous538487899
65852426658524267TTTCAA12GENIChomozygous697340842
65852426858524269GGC8GENIChomozygous697340843
65852426958524270TTTCA8GENIChomozygous697340844
65852504358525044GT23GENIChomozygous538487900
65852504658525047GA24GENIChomozygous538487901
65852627958526280TA36GENICpossibly homozygous541259336
65852628158526282TA36GENICpossibly homozygous541259337
65852696958526970TC22GENIChomozygous538487902
65852720058527201CT13GENIChomozygous538487903
65852860858528609TTAAA5GENIChomozygous697340846
65852875458528755GGA9GENIChomozygous697340847