chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1206711229206711230CCCCCA13GENIChomozygous61067603
1206711275206711276AG18GENIChomozygous61067604
1206711406206711407TG26GENIChomozygous61067605
1206711772206711773AG26GENIChomozygous61067606
1206712035206712036TC34GENIChomozygous61067607
1206712055206712056GC34GENIChomozygous61067608
1206712088206712089T-27GENIChomozygous61067609
1206712089206712090TC27GENIChomozygous62096241
1206712238206712239GA37GENIChomozygous61067610
1206712253206712254TC35GENIChomozygous61067611
1206712929206712930AG26GENIChomozygous61067612
1206713249206713250TTGAACTCA14GENIChomozygous61067613
1206713401206713402AG15GENIChomozygous61067614
1206713417206713418TC17GENIChomozygous61067615
1206713759206713760T-12GENICpossibly homozygous62193000
1206713943206713944CT18GENIChomozygous61067617
1206714020206714021GA15GENIChomozygous61067618
1206714363206714364CT21GENIChomozygous61067619
1206714622206714623TTA28GENIChomozygous61067620
1206714712206714713CT27GENIChomozygous61067621
1206714763206714775AAGCAAACAAAC------------18GENIChomozygous61067622
1206714879206714880AG28GENIChomozygous61067624
1206715036206715037TC25GENIChomozygous61067625
1206715108206715109CA29GENIChomozygous61067626
1206715360206715361TC24GENIChomozygous61067627
1206716182206716183TC20GENIChomozygous61067628
1206716363206716364CT18GENIChomozygous61067629
1206716513206716514AAGGCCTACCCGAGTAGTGTAAG24GENIChomozygous61067630
1206716612206716613AT16GENIChomozygous61067631
1206716877206716878CG30GENIChomozygous61067632