chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8116217744116217745CG10GENIChomozygous53305646
8116218666116218667CT3GENICheterozygous53305647
8116219174116219175GA9GENICpossibly homozygous53305648
8116219213116219214TC15GENICheterozygous53051252
8116219328116219329GA16GENICpossibly homozygous53305649
8116220478116220479TC15GENICpossibly homozygous53051256
8116221593116221594TC29GENICpossibly homozygous53051258
8116222693116222694AT21GENICpossibly homozygous52827676
8116222724116222725AG14GENIChomozygous52827677
8116223245116223246AT18GENICpossibly homozygous52827678
8116223318116223319CT9GENIChomozygous53305650