chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
33518974935189750GGC11GENICheterozygous58343961
33518990835189910AT--7GENIChomozygous57308635
33519043335190437AAAG----11GENIChomozygous57308638
33519045835190461AAG---27GENICheterozygous57308641
33519049635190497CA36GENICpossibly homozygous58343963
33519085235190853TTA23GENICpossibly homozygous58343965
33519087535190876G-25GENIChomozygous57308647
33519138735191391ACAC----4GENIChomozygous58343967
33519154035191542CC--14GENIChomozygous57308653
33519502635195027TTCACACA5GENIChomozygous57308664
33519565335195654G-14GENIChomozygous58279634
33519617835196181CCC---6GENICheterozygous58343969
33519622935196230TG21GENIChomozygous57308670
33519640335196404T-28GENICpossibly homozygous57308673
33519654835196549AATCTCTCTCTC6GENICheterozygous57308676
33519654835196549AATCTCTCTC6GENICheterozygous57308679
33519934435199345A-32GENIChomozygous57308688
33519938835199389AT44GENICpossibly homozygous58343971
33520006035200061AC9GENIChomozygous57308694
33520008035200081G-11GENIChomozygous57308697
33520008435200085AC13GENIChomozygous57886996