chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
17565218175652182TC16GENIChomozygous61441094
17565230775652308GA21GENICpossibly homozygous61441095
17565270375652704CG24GENIChomozygous61441096
17565288475652886AA--8GENIChomozygous61441097
17565305475653055AACG10GENICheterozygous62641772
17565377675653777CT10GENICpossibly homozygous61724878
17565379875653799CT9GENIChomozygous61724880
17565434875654349TA17GENIChomozygous61724882
17565443875654439TTGTGA1GENIChomozygous62718183
17565452075654521CA23GENIChomozygous61724886
17565463475654635GA19GENIChomozygous61724888
17565467175654672AG23GENICpossibly homozygous61724890
17565478275654783CG16GENICpossibly homozygous61724892
17565533175655332AG19GENICpossibly homozygous61724894
17565675775656758TC11GENIChomozygous61724896
17565681775656818T-18GENICpossibly homozygous61724898
17565694175656942GA15GENICpossibly homozygous61441105
17565779175657792TC10GENIChomozygous61441107
17565820675658207CT26GENIChomozygous61724902
17565905375659054AG2GENIChomozygous61724906
17566035375660354CT9GENICpossibly homozygous61724908
17566049975660500AG11GENICpossibly homozygous61724910
17566052975660530AACCC1GENIChomozygous62641773
17566053575660536TC1GENIChomozygous62641774
17566130975661310GT9GENIChomozygous61724912
17566158875661589C-1GENIChomozygous60740107
17566175475661755CT19GENIChomozygous61724914