chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1672212597221260TC13GENIChomozygous112049626
1672214797221480TC20GENIChomozygous112102870
1672222557222256GA18GENIChomozygous112049627
1672224507222451CT24GENIChomozygous112049628
1672224637222464GA27GENIChomozygous112049629
1672230707223071AG23GENIChomozygous112049630
1672236717223672GA23GENIChomozygous112049631
1672247297224730GA14GENIChomozygous112049632
1672253267225326AGTT19GENIChomozygous131743578
1672263207226321AG19GENIChomozygous112049633
1672292167229217TC17GENIChomozygous112049634
1672315787231592CAGAGTGCGTGGGA12GENIChomozygous132204403
1672323747232375TG8GENIChomozygous112049635
1672330957233096AG18GENIChomozygous112128100
1672355187235519GT21GENIChomozygous112049636
1672394907239491CT23GENIChomozygous112049637
1672397367239737CA18GENIChomozygous112049638
1672406117240612GA17GENICheterozygous119236182
1672407277240756GGGCTATCTCCCTGCAACACAGACCTCAC13GENICpossibly homozygous132427159
1672435687243569TC16GENIChomozygous112049639
1672441897244190GA16GENIChomozygous112049640
1672443387244339TA12GENIChomozygous112049641
1672446827244683GA18GENIChomozygous112049642
1672451097245110T16GENICpossibly homozygous131743583
1672463077246308GA16GENIChomozygous112049643
1672465067246507TC11GENIChomozygous112049644
1672484587248460GT15GENIChomozygous132204404
1672489567248957AG21GENIChomozygous112049645
1672497907249791TA14GENIChomozygous112049646
1672498527249860AGGACCAT20GENIChomozygous131743586
1672500457250046CT17GENIChomozygous112049647
1672507447250745GC12GENIChomozygous112049648