chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141752367817523679AAGCTCGATGATCACAAGATCTAATTTATGCTTAAGTTTCTTTGGACTGTCCATAACACTGTAGCTAT45GENIChomozygous49277966
141752371417523715AG19GENIChomozygous48548828
141752374517523746T-15GENIChomozygous48548829
141752376017523761TC14GENIChomozygous48548830
141752376617523767G-13GENIChomozygous48548831
141752377517523776T-16GENIChomozygous48548832
141752379117523792CA21GENIChomozygous48548833
141752380317523804TG27GENIChomozygous48548834
141752394117523942AAT32GENIChomozygous49277967
141752404917524050AT39GENIChomozygous48548836
141752425117524252TA34GENIChomozygous48548837
141752477217524773TC30GENIChomozygous48548838
141752526517525266GC37GENIChomozygous48548839
141752536317525364GA23GENIChomozygous48548840
141752542717525429TT--17GENIChomozygous48548841
141752576317525764GGGAGGACATTTACA11GENIChomozygous48548842
141752625017526251AAAC31GENIChomozygous48548845
141752658717526592TCTCC-----24GENIChomozygous48548846
141752698717526988TC33GENIChomozygous48548847
141752711017527111CT33GENIChomozygous48548848
141752766417527665TC24GENIChomozygous48548849
141752784917527850CT38GENIChomozygous48548850
141752855617528557CCT25GENIChomozygous48548851
141752867017528671CCT29GENIChomozygous48548852
141753100217531003GA42GENIChomozygous48548853
141753337517533376TC5GENIChomozygous48548854