chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
45046824150468242AG27GENIChomozygous56882640
45046843350468434TC24GENIChomozygous56882642
45046844550468446AG28GENIChomozygous56882644
45046871850468719TC32GENIChomozygous56882646
45046900350469004GA45GENIChomozygous56882648
45046938950469390GA43GENIChomozygous56882650
45047001750470018TC48GENIChomozygous56882652
45047009550470096AG45GENIChomozygous56882654
45047050350470504A-7GENICheterozygous56882657
45047050450470505CCTCT10GENICpossibly homozygous56882659
45047060350470604AT39GENIChomozygous56882661
45047064450470645AG50GENIChomozygous56882663
45047095150470952CT36GENIChomozygous56882665
45047123250471233CT51GENIChomozygous56882667
45047151150471512GGT30GENICpossibly homozygous56882669
45047172750471728AG43GENIChomozygous56882671
45047287550472876GT31GENIChomozygous56882673
45047341350473414T-24GENIChomozygous56882675
45047430150474302CT30GENICheterozygous57317267
45047430350474304CT29GENICheterozygous57317269
45047430550474306CT28GENICheterozygous57317271