chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106162422461624225CT38GENIChomozygous142253001
106164261261642612AT31GENICpossibly homozygous138686704
106165827661658277CA39GENIChomozygous138802466
106166397161663972GA50GENIChomozygous142253002
106167153061671531C3GENIChomozygous142204639
106168427961684280A23GENICheterozygous138686717
106168526261685263CT43GENIChomozygous142253003
106168528661685287CT46GENIChomozygous142253004
106168565161685652GA39GENIChomozygous138802494
106168583161685831TC42GENIChomozygous142204640
106168630361686304CT36GENIChomozygous138802496
106168637961686381GC46GENIChomozygous142204641
106168650561686506TG50GENIChomozygous138802497