chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103644998236449983CG10GENIChomozygous116759305
103645035236450353CG14GENIChomozygous116759307
103645125636451257TC11GENIChomozygous116759309
103645134836451349CG18GENICpossibly homozygous116759311
103645151836451519AG12GENIChomozygous116868309
103645159536451596GT18GENIChomozygous116759313
103645199036451991CT20GENIChomozygous116759315
103645200236452003GC20GENIChomozygous116759317
103645202836452029TC20GENIChomozygous116759319
103645207736452078GA17GENIChomozygous116759321
103645222236452223AG16GENIChomozygous116560949
103645225836452259GA16GENIChomozygous116759323