chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10110148567110148568AG45GENIChomozygous116719525
10110150641110150642CT49GENIChomozygous116719527
10110151026110151027AT39GENIChomozygous116719529
10110152178110152179TC49GENIChomozygous116719531
10110157027110157028CT51GENIChomozygous116719533
10110158438110158439CA3GENIChomozygous117035875
10110159900110159901TC31GENIChomozygous116719535
10110160865110160866AG19GENIChomozygous116719537
10110161337110161338TA40GENIChomozygous116719539
10110162051110162052CT45GENIChomozygous116719541
10110162692110162693GA53GENIChomozygous116719543
10110163180110163181TG36GENIChomozygous116719545
10110163833110163834AG61GENIChomozygous116719547
10110167423110167424TC20GENIChomozygous116719551
10110169700110169701GA17GENIChomozygous116719555
10110170030110170031TC41GENIChomozygous116719557
10110174535110174536GA41GENIChomozygous116719559
10110174617110174618GA31GENIChomozygous116719561
10110177688110177689CA44GENIChomozygous116719563
10110177786110177787AG31GENIChomozygous116719565
10110179313110179314AC15GENIChomozygous117035877
10110165556110165557CA16GENICheterozygous117280008