chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1199180076199180079GGG---8GENIChomozygous61043368
1199180369199180370AG26GENIChomozygous61799526
1199181566199181567CT44GENIChomozygous61799527
1199182678199182679AG28GENIChomozygous61799528
1199183709199183712TGT---19GENIChomozygous61799529
1199185845199185846AG38GENIChomozygous61043373
1199186378199186379AC26GENIChomozygous61043374
1199187469199187470TC29GENICpossibly homozygous61043376
1199187669199187670CT27GENIChomozygous61799530
1199188144199188145CT38GENIChomozygous61043377