chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
195539359455393595GA30GENIChomozygous109736780
195539402155394022TC26GENIChomozygous109736782
195539456455394565TC21GENIChomozygous109736784
195539665355396654AG13GENIChomozygous109736786
195539739955397400GA21GENIChomozygous109736788
195539949555399496CG20GENIChomozygous109736790
195540379555403796AG31GENIChomozygous109736792
195540404755404048GA26GENIChomozygous109736794
195540482455404825AG30GENIChomozygous109736796
195540485555404856CT23GENIChomozygous109736798
195540554455405545CT27GENIChomozygous109736800
195540577355405774GA24GENIChomozygous109736802
195540637955406380TC15GENIChomozygous109736804
195540733255407333CT16GENIChomozygous109736806
195540745055407451AG22GENIChomozygous109736808
195540824055408241GA15GENIChomozygous109736810
195540830155408302TC17GENIChomozygous109736812
195540855455408555CT13GENIChomozygous109736814
195540882055408821GA21GENIChomozygous109736816
195540890655408907AT18GENIChomozygous109736818
195541043355410434CG7GENIChomozygous109736822
195541113855411139CT13GENIChomozygous109736824
195541262155412622GT20GENIChomozygous109736826
195541384255413843TC15GENIChomozygous109736828
195541500155415002CT17GENIChomozygous109736830
195541591055415911CT21GENIChomozygous109736832
195541654255416543CT13GENIChomozygous109736834
195541668355416684GA17GENIChomozygous109736836
195541700555417006AG24GENIChomozygous109736838
195541716855417169AG20GENIChomozygous109736840
195541767255417673GA20GENIChomozygous109736842
195541768055417681TA16GENIChomozygous109736844
195541781355417814GC16GENIChomozygous109736846
195541860055418601TC20GENIChomozygous109736848
195541965955419660CT13GENIChomozygous109736850
195542089855420899TC20GENIChomozygous109736852
195542094855420949CT18GENIChomozygous109736854
195542110355421104GC23GENIChomozygous109736856
195542129955421300AG24GENIChomozygous109736858
195542190755421908GA19GENIChomozygous109736860
195541167155411672TA20GENIChomozygous109789014