chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
174542268145422682CA11GENIChomozygous47118713
174542279745422798CT25GENICpossibly homozygous47118714
174542334945423350AG14GENICpossibly homozygous47118715
174542393045423931AC19GENICpossibly homozygous47118716
174542617945426180CG23GENICpossibly homozygous47118717
174542730445427305CA12GENIChomozygous47118719
174542805945428060GA14GENICpossibly homozygous47118720
174542937545429376CCAA4GENIChomozygous47118726
174543097845430979TC7GENICheterozygous47118727
174543099445430995AG5GENIChomozygous47118728
174543236945432370CT18GENIChomozygous47118729
174543350045433501CT16GENICpossibly homozygous47118730
174543481745434818TC23GENIChomozygous47118731
174543558745435588AG20GENICpossibly homozygous47118732
174543590545435906GT3GENICheterozygous47118733
174543703145437032TC18GENIChomozygous47118734
174543717045437171GA12GENIChomozygous47118735
174543736945437370TG16GENIChomozygous47118736
174543761645437617TA5GENICheterozygous47118737