chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4149261124149261125AG21GENIChomozygous57516786
4149261125149261126GA21GENIChomozygous58285641
4149261548149261549TC8GENIChomozygous56977807
4149262047149262048CT20GENIChomozygous58086890
4149262850149262851CCTTCTCACAG34GENIChomozygous56977810
4149262868149262869GC30GENIChomozygous56977811
4149263165149263168TGT---26GENIChomozygous58086892
4149263197149263198GGGT30GENICpossibly homozygous57838730
4149264038149264039CT22GENIChomozygous58086894
4149264090149264091GA12GENIChomozygous56977816
4149264300149264306ATGTTT------21GENIChomozygous56977817
4149264309149264310AAG20GENIChomozygous56977818
4149264343149264344AT24GENIChomozygous56977819
4149264640149264641AG23GENIChomozygous56977820
4149264719149264720AT20GENICpossibly homozygous58086897
4149264856149264857TC29GENIChomozygous56977822
4149265082149265083CA23GENIChomozygous58086899
4149266377149266378AT23GENICpossibly homozygous56977829
4149267783149267785TG--15GENICheterozygous58528087
4149264147149264149CA--14GENIChomozygous58345745
4149264306149264307AC21GENIChomozygous58345747