chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
143815728638157287TG12GENIChomozygous113426634
143815745138157452TC16GENIChomozygous113426635
143815914938159150GT14GENIChomozygous113426636
143816150838161509TC18GENIChomozygous113426638
143816154038161541CA22GENIChomozygous113426639
143816156338161564AG8GENIChomozygous113426640
143816156638161567AG9GENIChomozygous113426641
143816162338161624AG7GENIChomozygous113426642
143816264838162649TC11GENIChomozygous113426643
143816281538162816TA11GENIChomozygous113426644
143816356038163561GA10GENIChomozygous113426645
143816410338164104AC7GENIChomozygous113426646
143816504738165048CT18GENIChomozygous113426647
143816539038165391CT23GENIChomozygous113426648
143816601238166013CT10GENIChomozygous113426649
143816603238166033AG17GENIChomozygous113426650
143816636638166367GA20GENIChomozygous113426651
143816699938167000TG12GENIChomozygous113426652
143816773338167734GA20GENIChomozygous113426653
143816811838168119TC8GENIChomozygous113426654
143816829538168296AC7GENIChomozygous113426655
143816830638168307GA8GENIChomozygous113426656
143816845238168453CG14GENIChomozygous113586972
143816941338169414GA12GENIChomozygous113426657
143816943538169436CT16GENIChomozygous113426658
143816957138169572GA19GENIChomozygous113426659
143817099838170999GT20GENIChomozygous113426660
143817102238171023CG18GENIChomozygous113426661
143816893238168933TG3GENICheterozygous125910949
143816883738168838AT7GENICheterozygous118688913