chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
64632721646327217CT21GENIChomozygous115381350
64632993046329931CT28GENICpossibly homozygous114787036
64632850646328507AT18GENIChomozygous114787028
64632920346329204CT24GENIChomozygous114787030
64632941346329414AT26GENIChomozygous114787032
64632979846329799CT27GENIChomozygous114787034
64633070546330706AG35GENIChomozygous114787042
64633241946332420TA22GENIChomozygous114787048
64633268346332684GA10GENIChomozygous115108863
64633316246333163CG30GENIChomozygous114787050
64633414246334143TC21GENICpossibly homozygous114787052
64633541846335419TC13GENIChomozygous114787056
64633552746335528GA43GENIChomozygous115108866
64633554446335545CA42GENICpossibly homozygous115108867
64633575846335759TC19GENIChomozygous114787058
64633575946335760GA19GENIChomozygous115108868
64633663446336635CT25GENIChomozygous114787062
64633785046337851CT18GENIChomozygous115381352
64633819046338191GA31GENIChomozygous114787068
64633910246339103AG28GENIChomozygous115381354
64633914146339142TC41GENIChomozygous115381356
64633986446339865AG30GENIChomozygous114787072
64633997746339978GA21GENIChomozygous115381358
64634098646340987CT24GENIChomozygous115381360
64634274446342745GT35GENIChomozygous114787094
64634332246343323GC39GENIChomozygous114787098
64634385646343857TG34GENIChomozygous114787100
64634395346343954AG32GENIChomozygous114787102
64634467246344673GA34GENIChomozygous114787104
64634542446345425GT36GENIChomozygous114787106
64634620146346202AG26GENIChomozygous114787108
64634687246346873CG20GENIChomozygous114787110