chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101047934510479346CCTTT18GENICheterozygous718104610
101047934510479346CCTTTT18GENICheterozygous718104611
101047966110479662C-17GENIChomozygous718104612
101047975810479759GT35GENIChomozygous584789782
101048004410480045GC52GENIChomozygous582729017
101048036610480367GC44GENIChomozygous582729018
101048130710481308GA42GENIChomozygous584789783
101048132310481324CA41GENIChomozygous584789784
101048148510481486CCCTTT18GENIChomozygous718104613
101048151810481521TTT---26GENICheterozygous718104615
101048151910481521TT--26GENICpossibly homozygous718104616
101048437010484371GA47GENIChomozygous584789785
101048679710486798CT66GENIChomozygous584789786
101048729410487295GC40GENIChomozygous582729019
101048929310489294CT32GENIChomozygous584789787
101049118910491190GT55GENIChomozygous582729020
101049179710491798TTA55GENIChomozygous718104618
101049546610495467AAGCACCAGATCTCATTACGGATGGTTGTGAGCCACCATGTGGTTGCTGGGGATTGAACTCATG11GENIChomozygous718104619
101049886610498867AG34GENIChomozygous582729021
101050028110500282TC41GENIChomozygous582729022
101050029410500295TG40GENIChomozygous582729023
101050176910501770TC36GENIChomozygous582729024
101050317710503178GA46GENIChomozygous582729025
101050397710503978TG49GENIChomozygous582729026
101050718410507185AG50GENIChomozygous582729027
101050910510509113CCTCTGCC--------14GENIChomozygous718104620
101051072210510723AG46GENIChomozygous582729028
101051149610511497AC53GENIChomozygous582729029
101051191910511920TC65GENIChomozygous582729030