chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
528564672856468TC29GENIChomozygous113627017
528566362856637AC30GENIChomozygous113627018
528570302857031AT18GENIChomozygous113627019
528571162857117TC18GENIChomozygous113627020
528586632858664GA31GENIChomozygous113627023
528591132859114TA33GENIChomozygous113627026
528600532860054GA26GENIChomozygous113627027
528618962861897CT22GENIChomozygous113627028
528621002862101CT25GENIChomozygous113627029
528626102862611CT25GENIChomozygous113627030
528632712863272GA24GENIChomozygous113627031
528634562863457GT21GENIChomozygous113627032
528642632864264CT30GENIChomozygous113627033
528661202866121AG23GENIChomozygous113627035
528665172866518CA26GENIChomozygous113627036
528683402868341GA25GENIChomozygous113627037
528685952868596GA32GENIChomozygous113627039
528687682868769GA28GENIChomozygous113627040
528689332868934AG26GENIChomozygous113627041
528689742868975TC25GENIChomozygous113627042
528699872869988TC20GENIChomozygous113627043
528717552871756AG27GENIChomozygous113627044
528736662873667GT27GENIChomozygous113627045
528745892874590TA20GENIChomozygous113627046
528752752875276CT31GENIChomozygous113627047
528756242875625GC20GENIChomozygous113627048
528759812875982AT17GENIChomozygous113627049
528762832876284TC20GENIChomozygous113627050
528783122878313GA19GENIChomozygous113627052