chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124053877140538772GA25GENIChomozygous115477561
124053976140539762GA25GENIChomozygous115328366
124054190040541901GT19GENIChomozygous115328370
124054419540544196AT19GENIChomozygous115383871
124054822740548228GT15GENIChomozygous115328380
124054822940548230GA15GENIChomozygous115328382
124054823340548234GA15GENIChomozygous115328384
124055777740557778TC24GENIChomozygous115477571
124055896640558967CA12GENIChomozygous115477573
124056103740561038TC13GENIChomozygous115328386
124056225540562256TC16GENIChomozygous115328388
124056451940564520TC20GENIChomozygous115328392
124056600840566009TC22GENIChomozygous115477575
124057097940570980CT11GENIChomozygous115477577
124057286140572862TG8GENIChomozygous115477581
124057318440573185TA4GENIChomozygous115583207
124057897740578978TC12GENIChomozygous115383883
124058060440580605AG19GENIChomozygous115328396
124058267040582671GA10GENIChomozygous115328398
124058288740582888AG9GENIChomozygous115328400
124058380440583805CT20GENICpossibly homozygous115441592
124058514740585148CT11GENIChomozygous115383885
124058538940585390CT5GENIChomozygous115328404
124058678740586788GA19GENIChomozygous115328406
124058990640589907AC26GENIChomozygous115441594
124057601540576016GC9GENIChomozygous115451469
124060899740608998TC17GENIChomozygous115328416
124060612540606126AG17GENIChomozygous115543984