chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
83918418139184182GA30GENICpossibly homozygous52961768
83918508239185083CG20GENICpossibly homozygous52961770
83918577639185777GA2GENIChomozygous52961772
83918621039186214GGGG----3GENICheterozygous52961776
83918660439186605AT24GENICpossibly homozygous52961778
83918718839187189TG4GENICheterozygous52961780
83918773639187737GA17GENICpossibly homozygous52961782
83918827639188277TC21GENIChomozygous52589957
83918865439188655GA16GENIChomozygous52961784
83918868539188697TTGTTTGTTTGT------------1GENIChomozygous52961786
83918873039188731TG17GENICpossibly homozygous52589962
83918888439188885GT7GENICheterozygous52589966
83918982239189823AG8GENIChomozygous52961790
83919061339190614GA15GENIChomozygous52961792
83919142939191430TC18GENIChomozygous52589995
83919199739191998AG11GENIChomozygous52961794
83919254139192542CA3GENICheterozygous52961796
83919254939192550AT2GENIChomozygous52961798
83919341939193420TG32GENIChomozygous52590009
83919579139195792TG26GENICheterozygous52961800
83919589339195894AACAGAC2GENICheterozygous52961802
83919676639196767AG14GENIChomozygous52590039
83919905739199058GA11GENIChomozygous52961804
83920014039200141GA7GENIChomozygous52961806
83920112839201129GA10GENICpossibly homozygous52961808
83920437839204379AC15GENIChomozygous52590119