chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104856968948569690A-4GENIChomozygous51640107
104857031448570315CCTTTCT5GENIChomozygous51640108
104857074448570745A-3GENICheterozygous52245819
104857141348571414TC9GENICpossibly homozygous51640109
104857142348571424GT9GENIChomozygous51640110
104857153448571535CCA11GENIChomozygous51447068
104857195948571960GA21GENICpossibly homozygous52055615
104857233548572336AG16GENICpossibly homozygous51640111
104857303548573036GT19GENICheterozygous51640112
104857352348573524TA24GENIChomozygous51640113
104857434748574348CT1GENIChomozygous51447070
104857441648574417CA4GENICheterozygous52318317
104857549748575498TC10GENICpossibly homozygous51640116
104857788848577889CA20GENICpossibly homozygous51640118
104857823448578235TC13GENICpossibly homozygous51640119
104857835448578355CT12GENICheterozygous52055619
104857900448579007TAA---1GENIChomozygous51640121
104857923748579238GGAA2GENICheterozygous51640122
104858182248581823GA9GENIChomozygous52055621
104858184048581841CT11GENIChomozygous52055623
104858190848581909GA17GENIChomozygous52055625
104858285548582856GA17GENICpossibly homozygous51640126
104858301548583016AG23GENICpossibly homozygous52055627
104858392448583936CTCTCTCCCCCC------------3GENICheterozygous52374364
104858436348584364T-9GENICheterozygous52055633
104858503448585035AG28GENIChomozygous52055635
104858532248585323TA14GENICpossibly homozygous52055637
104857873248578734AC--1GENIChomozygous51877449