chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
31911668819116689G12GENICheterozygous403058547
31911668819116689GC12GENICheterozygous403058548
31911669019116691G12GENICheterozygous403058549
31911669019116691GC12GENICheterozygous403058550
31912292719122928A12GENICheterozygous403058553
31912292719122928AG12GENICheterozygous403058554
31917938019179381AT8GENICheterozygous403058575
31917938019179381A8GENICpossibly homozygous403058576
31928790019287901TC17GENIChomozygous403058605
31928790019287901T17GENICheterozygous403058606
31928791219287913GT6GENICheterozygous403058607
31928791219287913G6GENIChomozygous403058608
31928791219287913GC6GENICheterozygous403058609
31932952319329524TC37GENICheterozygous154071443
31932952319329524T37GENICheterozygous403058623