chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4108140006108140007TG7GENIChomozygous112806630
4108180716108180717TG33GENIChomozygous119526714
4108462671108462672GT16GENIChomozygous112806658
4108493149108493150GT23GENICpossibly homozygous112806666
4108510136108510137AG15GENIChomozygous113151044
4108511942108511943AG28GENIChomozygous113151045
4108534140108534141GT4GENIChomozygous119438417
4108534170108534171CT16GENIChomozygous112806680
4108534176108534177CT23GENIChomozygous119370065
4108544929108544930AT12GENIChomozygous119279742
4108544930108544931TA12GENIChomozygous119279744
4108544935108544936GT10GENIChomozygous112806684
4108594461108594462CA26GENIChomozygous112806688
4108632963108632964GA20GENIChomozygous113151048
4108679402108679403GC17GENIChomozygous113046752
4108679451108679452GA19GENIChomozygous113046755
4108679452108679453TG19GENIChomozygous119457301
4108712049108712050CT3GENICheterozygous119454506
4108818495108818496GC17GENIChomozygous112806738
4108824757108824758GT29GENIChomozygous112806742
4108927619108927620GC22GENIChomozygous112806766
4108980925108980926TC30GENIChomozygous112806772
4109041447109041448TA19GENIChomozygous112806774