chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101396208313962084TC13INTERGENIChomozygous51622474
101396249013962491GA9INTERGENIChomozygous51622475
101396399013963991TA16INTERGENIChomozygous51622481
101396466513964666CT10INTERGENIChomozygous51622485
101396469213964693CT7INTERGENIChomozygous51622486
101396470913964710CT9INTERGENIChomozygous51622487
101396501213965013AG12INTERGENIChomozygous51622489
101396501513965016TC12INTERGENIChomozygous51622490
101396529513965296CG14INTERGENIChomozygous51622491
101396563613965637CT12INTERGENIChomozygous51622492
101396881013968811GA16INTERGENIChomozygous51622493
101396997713969978TA14INTERGENIChomozygous51622494
101397537713975378AAGTGTGCAT10INTERGENIChomozygous51622498
101397613313976134AG10INTERGENIChomozygous51622499
101397898213978983GA12INTERGENIChomozygous51622503
101398348813983489AT12INTERGENIChomozygous51622505
101398692513986926GA15INTERGENIChomozygous51622511
101398739713987398CT10INTERGENIChomozygous51622512
101399139013991391AC12GENIChomozygous51622515
101399165713991658AG9GENIChomozygous51622516
101399181113991812TC9GENIChomozygous51622518
101399190713991908TC18GENIChomozygous51622519
101399192913991930AG17GENIChomozygous51622520
101399352913993530CA17GENIChomozygous51622531
101399378113993782CT20GENIChomozygous51622532
101399578013995781CT12GENIChomozygous51622534
101399578213995783TC12GENIChomozygous51622535
101399593213995933TC17GENIChomozygous51622536
101399634913996350TC14GENIChomozygous51622538
101399642613996427T-14GENIChomozygous51622539