chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
172162929621629297TC18GENIChomozygous110988747
172162936221629363AG20GENIChomozygous110988749
172163040421630405AT35GENIChomozygous111178119
172163133821631339CT26GENIChomozygous110988753
172163140521631406TC30GENIChomozygous110988756
172163176521631766TC19GENIChomozygous110988758
172163201221632013TC16GENIChomozygous110988760
172163228621632287GA7GENIChomozygous110988762
172163241521632416CT17GENIChomozygous110988764
172163249221632493GA16GENIChomozygous110988766
172163251621632517TC16GENIChomozygous110988768
172163252621632527CT13GENIChomozygous110988770
172163252721632528AG13GENIChomozygous110988772
172163254721632548CT13GENIChomozygous110988774
172163265621632657AC20GENIChomozygous110988776
172163277121632772TC16GENIChomozygous110988778
172163306421633065TG28GENIChomozygous110988780
172163308421633085GC33GENIChomozygous110988782
172163312021633121AG25GENIChomozygous110988784
172163318321633184AG24GENIChomozygous110988786
172163321221633213AG26GENIChomozygous110988788
172163336321633364TA22GENIChomozygous110988790
172163336821633369GA20GENIChomozygous110988792
172163337021633371TC20GENIChomozygous110988794
172163339121633392TC28GENIChomozygous110988796
172163353521633536AG14GENIChomozygous110988798
172163356521633566CT10GENIChomozygous110988800
172163363121633632CT13GENIChomozygous110988802
172163370721633708CT17GENIChomozygous110988804
172163381121633812GA17GENIChomozygous111426236
172163388221633883AG24GENIChomozygous110988806
172163390821633909CT31GENIChomozygous110988808
172163392221633923AG29GENIChomozygous110988810
172163410521634106CT22GENIChomozygous110988812
172163418121634182CT25GENIChomozygous110988814
172163430221634303CT14GENICpossibly homozygous111234156
172163431721634318AG17GENIChomozygous111178121
172163442021634421TA24GENIChomozygous111426237