chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2233604981233604981G13GENIChomozygous131303023
2233605147233605148GC20GENIChomozygous110310901
2233605784233605784G11GENIChomozygous127749298
2233607537233607538CA20GENIChomozygous110837632
2233607870233607871CT18GENIChomozygous110310905
2233608223233608223A19GENIChomozygous131303024
2233608593233608594CG26GENIChomozygous110310911
2233609230233609231TA4GENIChomozygous110310913
2233609391233609392AT24GENIChomozygous110837633
2233610088233610089CT19GENIChomozygous110310915
2233612250233612251GA19GENIChomozygous110310917
2233612388233612388AC17GENIChomozygous131303025
2233612761233612762AT14GENIChomozygous110837635
2233613635233613636GT24GENIChomozygous110310921
2233613661233613662CG25GENIChomozygous110310923
2233614053233614053C18GENIChomozygous127749301
2233614061233614062CA18GENIChomozygous110310925
2233614977233614978T1GENIChomozygous131303026
2233616021233616022AG15GENIChomozygous110310929
2233617390233617391AG16GENIChomozygous110310931
2233617474233617475GA18GENIChomozygous110310933
2233618392233618393GT15GENIChomozygous110837637
2233618517233618518AT19GENIChomozygous110837639
2233618824233618826AG21GENIChomozygous131303027
2233618998233618999CT18GENIChomozygous110837641
2233619337233619337GGCTGGGTCC10GENIChomozygous131303028
2233619615233619616GA14GENIChomozygous110837643
2233619625233619626TC16GENIChomozygous110837645
2233618105233618106AG26GENIChomozygous120161739