chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
182456030324560304GA29GENIChomozygous110582834
182456283624562837AG21GENIChomozygous110582836
182456290824562909TC28GENIChomozygous110582838
182456294024562941AT24GENIChomozygous110582840
182456422424564225TA21GENIChomozygous110582842
182456464824564649CA22GENIChomozygous110582844
182456490524564906CA32GENIChomozygous110582846
182456507424565075AG36GENIChomozygous110582848
182456733224567333TC20GENIChomozygous110582850
182456778724567788CT23GENIChomozygous110582852
182456853024568531AG18GENIChomozygous110582854
182456920424569205AG18GENIChomozygous110582856
182456986124569862TA11GENIChomozygous110582858
182457047724570478CA24GENIChomozygous110582860
182456595524565956GA18GENICpossibly homozygous110723420
182456623524566236TC27GENIChomozygous110744720
182456883024568831GA21GENICheterozygous119553372