chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
161896149518961496TC28GENIChomozygous112275068
161896212918962130G46GENIChomozygous131173613
161896253718962537GCTGG35GENIChomozygous131173614
161896545418965455GA44GENIChomozygous111945713
161896556218965563AG40GENIChomozygous111945716
161896777318967774AG40GENIChomozygous111945718
161896950818969509TG61GENIChomozygous111945720
161897255718972557G46GENIChomozygous131173615
161897255818972559AG47GENIChomozygous111945722
161897355018973551TA52GENIChomozygous111945724
161897481518974815T52GENIChomozygous131173616
161897481918974820TC53GENIChomozygous111945726
161897030918970310AG20GENIChomozygous119192578
161897032418970324A8GENICheterozygous130452439
161897296818972969AG45GENIChomozygous111750530
161896801318968014G16GENIChomozygous129339752