chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
144411464444114645GA43GENIChomozygous65948312
144411465644114657GA41GENIChomozygous65948314
144411489944114900AG64GENIChomozygous65948316
144411495644114957AG73GENIChomozygous65948318
144411551544115516AC57GENIChomozygous65948320
144411564844115649AC56GENIChomozygous65948322
144411610544116106GA40GENIChomozygous65948324
144411614244116143CA43GENIChomozygous65948326
144411630244116303CG18GENIChomozygous65948328
144411636844116369AG28GENICpossibly homozygous65948330
144411646044116461GA51GENIChomozygous65948332
144411672544116726CT66GENIChomozygous65948334
144411676044116761AG60GENIChomozygous65948336
144411707444117075CT49GENIChomozygous65948338
144411783644117837GA39GENIChomozygous65948340
144411787544117876AG53GENIChomozygous65948342
144411806144118062TC39GENIChomozygous65948344
144411817844118179GC57GENIChomozygous65948346
144411894744118948CT56GENICpossibly homozygous65948348
144411905144119052GA44GENIChomozygous65948350
144411943344119434TA58GENIChomozygous65948352
144412005844120059CT51GENIChomozygous65948354
144412014144120142TC54GENIChomozygous65948356
144412050044120501GA61GENIChomozygous65948358
144412159044121591GA47GENIChomozygous65948360
144412160244121603TC52GENIChomozygous65948362
144412282444122825CA26GENICpossibly homozygous65948364
144412311544123116TG39GENIChomozygous65948366
144412457144124572AG42GENIChomozygous65948368