chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
83918508239185083CG32GENIChomozygous52961770
83918577639185777GA19GENIChomozygous52961772
83918599539185998AAA---11GENICpossibly homozygous52961774
83918599639185998AA--11GENICheterozygous52589938
83918660439186605AT23GENIChomozygous52961778
83918718839187189TG24GENIChomozygous52961780
83918827639188277TC30GENIChomozygous52589957
83918865439188655GA14GENIChomozygous52961784
83918868539188697TTGTTTGTTTGT------------11GENIChomozygous52961786
83918873039188731TG19GENIChomozygous52589962
83918888439188885GT18GENIChomozygous52589966
83918942439189425CG19GENIChomozygous53101522
83918977739189789ACACACACACAC------------7GENICheterozygous53651449
83918982239189823AG15GENIChomozygous52961790
83919016339190164GGGA34GENIChomozygous53101524
83919048139190482GGACACAC7GENICheterozygous52589985
83919048139190482GGACACACAC7GENICheterozygous53428135
83919061339190614GA33GENIChomozygous52961792
83919142939191430TC13GENIChomozygous52589995
83919199739191998AG24GENIChomozygous52961794
83919254139192542CA19GENIChomozygous52961796
83919254939192550AT21GENIChomozygous52961798
83919341939193420TG18GENIChomozygous52590009
83919533439195335GA24GENIChomozygous53101525
83919579139195792TG23GENIChomozygous52961800
83919589339195894AACAGAC9GENIChomozygous52961802
83919676639196767AG19GENIChomozygous52590039
83919905739199058GA37GENIChomozygous52961804
83919985339199854TC18GENIChomozygous53101526
83920014039200141GA12GENIChomozygous52961806
83920112839201129GA21GENIChomozygous52961808
83920181239201813AAAGAG10GENICpossibly homozygous53101527
83920181239201813AAAGAGAG10GENICheterozygous53610679
83920186639201870GAAT----15GENIChomozygous53101528
83920290839202909A-12GENICheterozygous52590104
83920343739203438AAACAC3GENIChomozygous52590111
83920405239204053GA16GENIChomozygous53101529
83920437839204379AC10GENIChomozygous52590119