chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108551133485511335GA22GENIChomozygous53160698
108551134685511347CT23GENIChomozygous51526084
108551144285511443CT30GENICpossibly homozygous53160700
108551253485512535TTA12GENIChomozygous51526086
108551260585512609AAAA----4GENICheterozygous53160702
108551262085512621AACC5GENICheterozygous53160704
108551265685512657AG14GENIChomozygous53160706
108551349185513492TC27GENIChomozygous51526088
108551368385513684T-35GENIChomozygous52571173
108551384685513847AG37GENICpossibly homozygous51526089
108551404185514042G-36GENICpossibly homozygous51526090
108551448785514488GA20GENIChomozygous53160708