chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1243024699243024700AG25GENIChomozygous135851842
1243024920243024921TC34GENIChomozygous135851843
1243025642243025643CT22GENIChomozygous135851844
1243025772243025772T3GENIChomozygous135469580
1243026257243026257TGT24GENIChomozygous135469581
1243027956243027957AG16GENIChomozygous135851848
1243028117243028118AC33GENIChomozygous135851849
1243028764243028765A18GENIChomozygous135469582
1243028776243028777GA25GENIChomozygous135851850
1243029808243029809TC46GENIChomozygous135851851
1243030442243030443GA36GENIChomozygous135851853
1243030473243030474CT32GENIChomozygous135851854
1243030512243030513CT28GENIChomozygous135851855
1243030587243030588TC21GENIChomozygous135851856
1243031412243031413T13GENIChomozygous135469583
1243031453243031454AG15GENIChomozygous135851857
1243031685243031686CT34GENIChomozygous141305324
1243028244243028245A23GENICheterozygous149514745
1243028244243028245AC23GENIChomozygous153910875