chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
155897835258978353TA30GENIChomozygous48321099
155898293658982937TTG14GENICpossibly homozygous48768068
155898293858982940GG--14GENICheterozygous48961058
155898685058986852AA--9GENICheterozygous49244918
155898685158986852A-9GENICheterozygous49164558
155898745058987451TC28GENIChomozygous48961072
155898745158987452CA28GENIChomozygous49055436
155898745358987454TTA28GENIChomozygous48321119
155898746158987462TTA31GENIChomozygous48321120
155898747558987476GGT32GENIChomozygous48321121
155899523558995236CCCAAACAAA16GENIChomozygous49221308
155899879658998797CT35GENIChomozygous48321149
155899969258999693AT17GENIChomozygous48321151
155899969558999696AT18GENIChomozygous48768070
155900078559000794GGCGGCGGC---------26GENIChomozygous48321154
155900089759000898A-28GENIChomozygous48321155