chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
18401931484019315CT29GENIChomozygous108879875
18401957784019578GA41GENIChomozygous108879876
18401963584019636GA46GENIChomozygous108879877
18401985284019853CT26GENIChomozygous108879878
18402108584021086GA26GENIChomozygous108879879
18402153884021539AG23GENIChomozygous108879885
18402217884022179AT38GENIChomozygous108879886
18402218084022181GA38GENIChomozygous108879887
18402251184022512GA25GENIChomozygous108879888
18402337884023379AG25GENIChomozygous108879889
18402359384023594GA32GENIChomozygous108879890
18402423384024234AC21GENIChomozygous108879891
18402522584025226GT29GENIChomozygous108879892
18402625584026256TC22GENIChomozygous108879893
18402656684026567AG26GENIChomozygous108879894
18402676284026763CA38GENIChomozygous108879895
18402709384027094AG31GENIChomozygous108879896
18402750384027504GA13GENIChomozygous108879897
18402815084028151TA37GENIChomozygous108879898
18403111584031116AG28GENIChomozygous108879900
18403113084031131TG30GENIChomozygous108879901
18403189884031899AT36GENIChomozygous108879902
18403348184033482TC42GENIChomozygous108879904
18403381884033819TC12GENIChomozygous108879905
18403445084034451AG23GENIChomozygous108879906
18403491384034914AG35GENICpossibly homozygous108879907
18403502584035026TC28GENIChomozygous108879908
18402051384020514TC30GENIChomozygous120514120
18402231884022318C19GENIChomozygous131259067
18402254284022542T22GENIChomozygous131259068
18402670284026703A27GENIChomozygous131259069
18403266684032667T20GENICheterozygous132932176
18403648784036488TG30GENIChomozygous108879909
18403693584036936AG26GENIChomozygous108879910
18403730684037307AG38GENIChomozygous108879911
18403786784037868A32GENIChomozygous131259070
18403815784038157A30GENIChomozygous131259071
18403823084038231AT30GENIChomozygous108879912
18403841484038415AG26GENICpossibly homozygous108879913
18404020184040202GA24GENIChomozygous120667207