chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
162486311324863114CCGT21GENIChomozygous694742097
162486313224863133TA23GENIChomozygous530868719
162486320324863204TA24GENIChomozygous529781801
162486376124863762GA13GENIChomozygous530868720
162486389124863892GC17GENIChomozygous529781802
162486399024863991GGT15GENIChomozygous694742098
162486527524865276A-34GENIChomozygous694742099
162486561624865617CT20GENIChomozygous529781803
162486567624865677TC22GENICheterozygous530868721
162486670024866701TC13GENIChomozygous530868722
162486680224866803CT16GENICpossibly homozygous530868723
162486702724867028CCT30GENIChomozygous694742100
162486775724867758AG24GENIChomozygous530868724
162486855024868551CT29GENIChomozygous529781804
162486918724869188CT13GENIChomozygous530868725
162486920124869202GA13GENIChomozygous530868726
162486940724869408TA16GENIChomozygous529781805
162486964924869653TAAG----11GENIChomozygous694742101
162486971724869718GC12GENIChomozygous530868727
162486974824869749A-13GENIChomozygous694742102
162487027424870275CG18GENIChomozygous530868728
162487135524871356CG6GENIChomozygous529781806
162487156524871566TA10GENICheterozygous530868729
162487169924871700CT12GENICheterozygous530868730
162487173724871738CA16GENICheterozygous530868731
162487185724871858AC10GENICheterozygous530868732
162487186724871868CG7GENICheterozygous530868733