chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
45768504357685044TC32GENICpossibly homozygous113025612
45768881357688814CT20GENIChomozygous113025613
45768932857689329AG19GENICpossibly homozygous112659306
45768971257689713GC31GENICpossibly homozygous113025615
45769003557690036CT23GENIChomozygous113025616
45769009357690094TG19GENIChomozygous112659308
45769013357690134AG23GENIChomozygous113025617
45769064757690648CT34GENIChomozygous113025618
45769120457691205AC27GENIChomozygous113025619
45769203957692040GA30GENIChomozygous113025620
45769303657693037TC23GENIChomozygous112659312
45769523957695240TC31GENIChomozygous113025621
45769748957697490GA13GENIChomozygous113025623
45769794457697945TC26GENIChomozygous112659313
45769869557698696CA35GENIChomozygous113025624
45769961257699613CT24GENIChomozygous113025625
45770166557701666AG7GENIChomozygous113025626
45770225457702255CT18GENIChomozygous113025627
45770258357702584AG26GENIChomozygous113025629
45770276357702764CG26GENIChomozygous113025630
45770319257703193TC29GENIChomozygous113025632
45770449457704495AG25GENICpossibly homozygous113025633
45770480057704801TA13GENIChomozygous113025634
45770636857706369CG18GENIChomozygous113025635
45770645357706454CT16GENIChomozygous112659319
45770660057706601CG12GENIChomozygous113025636
45770660657706607TA13GENICpossibly homozygous113025637