chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
22504052925040530AG20GENIChomozygous109649054
22504150425041505AG6GENIChomozygous109649055
22504195525041956TA6GENIChomozygous109649057
22504200425042005TA7GENIChomozygous109649059
22504234725042348GA16GENIChomozygous109649061
22504240325042404AG18GENIChomozygous109649063
22504255825042559CT15GENIChomozygous109649065
22504263025042631CT20GENIChomozygous120122358
22504298525042986CT22GENIChomozygous109649067
22504329725043298GC24GENIChomozygous109649069
22504341825043419GT34GENIChomozygous109649071
22504385325043854CT17GENIChomozygous109649075
22504393125043932CT9GENIChomozygous109649077
22504457825044579CT12GENIChomozygous109649079
22504500525045006TG28GENIChomozygous110675498
22504533525045336AG24GENIChomozygous109649085
22504539825045399GA19GENIChomozygous110675500
22504545025045451TC22GENIChomozygous109649087
22504549825045499AG23GENIChomozygous109649089
22504631225046313CT17GENIChomozygous110490942
22504661825046619AG20GENIChomozygous110490944
22504681025046811CA34GENIChomozygous109649095
22504693425046935TC28GENIChomozygous110490946
22504712725047128CT30GENIChomozygous109649098
22504714625047147AC31GENIChomozygous110490948
22504715425047155TC31GENIChomozygous109649100
22504718425047185CT29GENIChomozygous109649102
22504726825047269CT26GENIChomozygous110490950
22504783525047836CG19GENIChomozygous110490954
22504804825048049CT18GENIChomozygous110490956
22504815225048153CT16GENIChomozygous109649110
22504833825048339GT20GENIChomozygous109649112
22504839725048398AG16GENIChomozygous109649114
22504936425049365AG17GENIChomozygous109649118
22504948925049490CG26GENIChomozygous110675502
22504984325049844CT25GENIChomozygous109649122
22504989325049894GA25GENIChomozygous110675504
22505046025050461CG16GENIChomozygous109649126
22505049125050492GC16GENIChomozygous109649128
22505092925050930AG13GENIChomozygous109649130
22505149125051492AG12GENIChomozygous110675508