chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1243024699243024700AG63GENIChomozygous135851842
1243024920243024921TC64GENIChomozygous135851843
1243025642243025643CT63GENICpossibly homozygous135851844
1243025772243025772T10GENICpossibly homozygous135469580
1243026257243026257TGT56GENIChomozygous135469581
1243027779243027780CT47GENIChomozygous135851845
1243027834243027835TC44GENIChomozygous135851846
1243027875243027876CT32GENIChomozygous135851847
1243027956243027957AG33GENIChomozygous135851848
1243028117243028118AC54GENIChomozygous135851849
1243028764243028765A57GENICpossibly homozygous135469582
1243028776243028777GA57GENIChomozygous135851850
1243029808243029809TC64GENIChomozygous135851851
1243030031243030032CT51GENIChomozygous135851852
1243030442243030443GA60GENIChomozygous135851853
1243030473243030474CT57GENIChomozygous135851854
1243030512243030513CT57GENIChomozygous135851855
1243030587243030588TC51GENIChomozygous135851856
1243031412243031413T50GENIChomozygous135469583
1243031453243031454AG42GENIChomozygous135851857
1243028244243028245AC49GENIChomozygous153910875
1243028244243028245A49GENICheterozygous149514745