chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108364575483645755CT29GENIChomozygous51520727
108364845583648456CG27GENIChomozygous51520735
108364866683648667CCTTT1GENIChomozygous51520736
108364950083649501AG27GENIChomozygous51520738
108364984683649847AG28GENIChomozygous51520739
108365024183650242CCTT8GENIChomozygous51520741
108365063583650636GGT29GENIChomozygous51720546
108365076983650770TC33GENIChomozygous51520743
108365289183652893AA--15GENICheterozygous51720550
108365289283652893A-15GENICpossibly homozygous51520746
108365310983653110CG28GENICheterozygous51520747