chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7108388433108388434TC59GENIChomozygous138177764
7108388792108388793CT56GENIChomozygous138177765
7108388970108388971TC57GENIChomozygous138177766
7108389579108389580CT59GENIChomozygous138177767
7108390785108390785AAG27GENICheterozygous137973321
7108390786108390786AG29GENICpossibly homozygous137973322
7108390815108390816TA38GENIChomozygous138177768
7108391141108391142GA57GENIChomozygous138177769
7108391547108391548TC49GENIChomozygous138177770