chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
172162798721627988TA6GENIChomozygous110988745
172162929621629297TC7GENIChomozygous110988747
172162936221629363AG24GENIChomozygous110988749
172163016021630161TC15GENIChomozygous110988751
172163040421630405AT9GENIChomozygous111178119
172163133821631339CT6GENIChomozygous110988753
172163140521631406TC17GENIChomozygous110988756
172163176521631766TC14GENIChomozygous110988758
172163201221632013TC10GENIChomozygous110988760
172163228621632287GA4GENIChomozygous110988762
172163241521632416CT9GENIChomozygous110988764
172163249221632493GA9GENIChomozygous110988766
172163251621632517TC10GENIChomozygous110988768
172163277121632772TC14GENIChomozygous110988778
172163252621632527CT11GENIChomozygous110988770
172163252721632528AG11GENIChomozygous110988772
172163254721632548CT13GENIChomozygous110988774
172163265621632657AC19GENIChomozygous110988776
172163306421633065TG20GENIChomozygous110988780
172163308421633085GC13GENIChomozygous110988782
172163312021633121AG15GENIChomozygous110988784
172163318321633184AG26GENIChomozygous110988786
172163321221633213AG25GENIChomozygous110988788
172163336321633364TA10GENIChomozygous110988790
172163336821633369GA9GENIChomozygous110988792
172163337021633371TC10GENIChomozygous110988794
172163339121633392TC12GENIChomozygous110988796
172163353521633536AG23GENIChomozygous110988798
172163356521633566CT20GENIChomozygous110988800
172163363121633632CT19GENIChomozygous110988802
172163370721633708CT15GENIChomozygous110988804
172163388221633883AG25GENIChomozygous110988806
172163390821633909CT28GENIChomozygous110988808
172163392221633923AG28GENIChomozygous110988810
172163410521634106CT23GENIChomozygous110988812
172163418121634182CT27GENICpossibly homozygous110988814
172163430221634303CT27GENIChomozygous111234156
172163431721634318AG24GENIChomozygous111178121