chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
18273419882734199CT16GENIChomozygous61450643
18273438782734388TA18GENIChomozygous61450644
18273512182735123GG--22GENIChomozygous61450645
18273527782735278AG15GENIChomozygous61450646
18273568082735681GGT16GENIChomozygous60747210
18273617182736172AG18GENICheterozygous62480668
18273639482736395GT26GENIChomozygous61450648
18273641582736416AG27GENIChomozygous61450649
18273946782739468GA19GENIChomozygous61450656
18274020982740210TA9GENIChomozygous61450657
18274045382740454CT17GENIChomozygous61450658
18274048782740488TTGTGCGCATGCCTGTGTGC12GENIChomozygous62551715
18274050782740512AACAA-----24GENIChomozygous62137519
18274051182740512AAGGTGC23GENIChomozygous62137520
18274136382741365GG--17GENICheterozygous60747213
18274136482741365G-17GENICheterozygous60747214
18274156282741563CCTGTG14GENIChomozygous61450662
18274253682742537A-15GENIChomozygous61450663
18274254982742550A-19GENIChomozygous61450664
18274256582742566CCA12GENICpossibly homozygous61450665
18274300582743009TTAT----22GENIChomozygous61450666
18274301782743018AT23GENIChomozygous61450667
18274398082743981TA17GENIChomozygous61450668
18274444182744443CT--6GENIChomozygous62137525
18274560782745608AG13GENIChomozygous61450669
18274579982745800CT21GENIChomozygous61450670
18274599382745994TC18GENIChomozygous61450671
18274690282746903AC24GENIChomozygous61450672
18274716782747168G-18GENIChomozygous61450673
18274786482747865AG27GENIChomozygous61450674
18274788182747882CG26GENIChomozygous61450675
18274797782747978TTACACAC11GENIChomozygous62551717
18274917082749171CCTTAT5GENIChomozygous62259930
18274919082749191TA7GENIChomozygous61450677
18274919882749199TA7GENIChomozygous61450678
18274943682749437A-11GENIChomozygous61450680
18274997082749971AG20GENIChomozygous61450681