chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
135578919955789201TC--2GENICheterozygous707810766
135578961855789622TCTC----1GENIChomozygous707810769
135579103355791034GA12GENICheterozygous562160624
135579303055793031AG7GENICpossibly homozygous562160625
135579307355793074T-4GENICheterozygous707810772
135579400355794004GA2GENIChomozygous564887153
135579446155794462CT19GENIChomozygous562160626
135579512755795128AG25GENIChomozygous562160627
135579527055795271CT4GENIChomozygous562160628
135579548355795484TC19GENICpossibly homozygous562160629
135579568655795687GGC19GENICpossibly homozygous707810773
135579597255795973GA18GENICpossibly homozygous562160630
135579808655798087AG5GENIChomozygous564887154
135579830955798310TTG6GENICheterozygous707810774
135579909955799100AC18GENIChomozygous562160631
135579987755799878AG9GENICheterozygous562160632
135580062355800624CG21GENICpossibly homozygous562160633
135580164955801650AG27GENIChomozygous562160634
135580172555801726AG18GENIChomozygous562160635