chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141752368017523681TC14GENICheterozygous48548827
141752371417523715AG14GENIChomozygous48548828
141752374517523746T-14GENIChomozygous48548829
141752376017523761TC14GENIChomozygous48548830
141752376617523767G-10GENIChomozygous48548831
141752377517523776T-9GENIChomozygous48548832
141752379117523792CA12GENIChomozygous48548833
141752380317523804TG16GENIChomozygous48548834
141752394217523950GGTACGGT--------15GENIChomozygous48548835
141752404917524050AT29GENIChomozygous48548836
141752425117524252TA16GENIChomozygous48548837
141752477217524773TC25GENIChomozygous48548838
141752526517525266GC13GENIChomozygous48548839
141752536317525364GA8GENIChomozygous48548840
141752542717525429TT--8GENIChomozygous48548841
141752576317525764GGGAGGACATTTACA28GENIChomozygous48548842
141752576517525766TA30GENICheterozygous48548843
141752625017526251AAAC15GENIChomozygous48548845
141752658717526592TCTCC-----10GENIChomozygous48548846
141752698717526988TC15GENIChomozygous48548847
141752711017527111CT14GENIChomozygous48548848
141752766417527665TC19GENICpossibly homozygous48548849
141752784917527850CT20GENIChomozygous48548850
141752855617528557CCT11GENIChomozygous48548851
141752867017528671CCT10GENIChomozygous48548852
141753100217531003GA17GENIChomozygous48548853
141753337517533376TC33GENIChomozygous48548854