chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
148931479189314792TC9GENIChomozygous113509559
148931797989317980TC22GENIChomozygous113509561
148931978489319785AG27GENIChomozygous113509563
148931980189319802TC24GENIChomozygous113509565
148931982089319821TA24GENIChomozygous113509567
148932007389320074TC34GENIChomozygous113509569
148932020789320208CT24GENIChomozygous113509571
148932056789320568AC19GENIChomozygous113509573
148932112089321121TC21GENIChomozygous113509575
148932153889321539AG32GENIChomozygous113509577
148932202189322022CT21GENIChomozygous113509579
148932308489323085TC12GENIChomozygous113610256
148932640189326402CT9GENIChomozygous113509581
148932668089326681AG16GENIChomozygous113509583
148932812689328127GC20GENIChomozygous113509585
148932863489328635AC18GENIChomozygous113509587
148932870089328701TC18GENIChomozygous113509589
148932870789328708TA21GENIChomozygous113509591
148932872589328726TC22GENIChomozygous113509593
148932873389328734AC23GENIChomozygous113509595
148932960589329606AG10GENIChomozygous113509597
148932961289329613CT10GENIChomozygous113610272
148933024489330245TA8GENIChomozygous113509599
148933040289330403GT21GENICpossibly homozygous113509601
148933045389330454GT18GENIChomozygous113509603
148933054089330541CT25GENIChomozygous113509605
148933072589330726GT19GENIChomozygous113509607
148933123089331231TC28GENIChomozygous113509609
148933138989331390TC26GENIChomozygous113509611
148933143589331436AG17GENIChomozygous113509613
148933168089331681CG22GENIChomozygous113509615
148933168789331688TC20GENIChomozygous113509617
148933216789332168CA16GENIChomozygous113509619
148933246289332463TG18GENIChomozygous113509621
148933250589332506TG20GENIChomozygous113509623
148933272289332723TC13GENIChomozygous113509625
148933273289332733CT13GENIChomozygous113509627
148933293689332937TC15GENIChomozygous113509629
148933299689332997AG10GENIChomozygous113509631
148933369789333698CT13GENIChomozygous113509633