chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101396208313962084TC17INTERGENIChomozygous51622474
101396249013962491GA8INTERGENIChomozygous51622475
101396399013963991TA12INTERGENIChomozygous51622481
101396466513964666CT13INTERGENIChomozygous51622485
101396469213964693CT16INTERGENIChomozygous51622486
101396470913964710CT16INTERGENIChomozygous51622487
101396494413964945AT16INTERGENIChomozygous51622488
101396501213965013AG25INTERGENIChomozygous51622489
101396501513965016TC27INTERGENIChomozygous51622490
101396529513965296CG15INTERGENIChomozygous51622491
101396563613965637CT19INTERGENIChomozygous51622492
101396881013968811GA22INTERGENIChomozygous51622493
101396997713969978TA16INTERGENIChomozygous51622494
101397017213970173AAAAGG14INTERGENIChomozygous51622495
101397537713975378AAGTGTGCAT12INTERGENIChomozygous51622498
101397613313976134AG11INTERGENIChomozygous51622499
101397710513977106AG12INTERGENIChomozygous51622500
101397898213978983GA11INTERGENIChomozygous51622503
101398348813983489AT20INTERGENIChomozygous51622505
101398692513986926GA22INTERGENIChomozygous51622511
101398739713987398CT24INTERGENIChomozygous51622512
101398983313989834AAT13INTERGENIChomozygous51622514
101399139013991391AC9GENIChomozygous51622515
101399165713991658AG24GENIChomozygous51622516
101399190713991908TC21GENIChomozygous51622519
101399192913991930AG22GENIChomozygous51622520
101399352913993530CA17GENIChomozygous51622531
101399378113993782CT12GENIChomozygous51622532
101399511713995118T-10GENIChomozygous51622533
101399578013995781CT13GENIChomozygous51622534
101399578213995783TC13GENIChomozygous51622535
101399593213995933TC16GENIChomozygous51622536
101399634913996350TC18GENIChomozygous51622538
101399642613996427T-20GENIChomozygous51622539