chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1254222000254222003AGA25GENIChomozygous135474416
1254222267254222268CT17GENIChomozygous135872755
1254222271254222272GA19GENICpossibly homozygous135872756
1254222485254222486CT13GENIChomozygous135872757
1254222806254222807TC26GENIChomozygous135872758
1254223405254223406TC12GENIChomozygous135872759
1254223827254223828GA12GENIChomozygous135872760
1254224747254224748GA30GENIChomozygous135872761
1254226150254226151CT26GENIChomozygous135872762
1254226875254226876AG20GENIChomozygous135872763
1254226953254226954CG16GENIChomozygous135872764
1254227758254227759TG18GENIChomozygous135872765
1254229165254229166TC18GENIChomozygous135872766
1254229950254229951TC20GENIChomozygous135872767
1254230022254230036TCAAGGAATGAATG16GENIChomozygous135474417
1254230936254230937AG18GENIChomozygous135872768
1254231692254231693TC17GENIChomozygous135872769
1254231889254231889G16GENIChomozygous135474418
1254232555254232556CT18GENIChomozygous135872770
1254234117254234119TC19GENIChomozygous135474419
1254234756254234757CT26GENIChomozygous135872771
1254235269254235270CT16GENIChomozygous135872772
1254236054254236055CT25GENIChomozygous135872773
1254236294254236295AG17GENIChomozygous135872774