chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1127557821127557821T44GENIChomozygous127427861
1127557832127557832T42GENIChomozygous127427862
1127557835127557836G39GENIChomozygous127427863
1127557841127557842A38GENIChomozygous127427864
1127557846127557847A35GENIChomozygous127427865
1127557850127557850C36GENIChomozygous127427866
1127594078127594079A63GENIChomozygous127427868
1127594104127594104A63GENIChomozygous127427869
1127594111127594111G65GENIChomozygous127427870
1127594156127594158CT47GENIChomozygous127427871
1127594167127594167TG37GENIChomozygous127427872
1127595856127595857GA39GENIChomozygous109136382
1127595858127595858G40GENIChomozygous127427873
1127594092127594093CT65GENIChomozygous108223652
1127594399127594400AC66GENIChomozygous108223654
1127594400127594401AC66GENIChomozygous108223656