chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2248737327248737328CT14GENIChomozygous110372474
2248739474248739475CT16GENIChomozygous110372476
2248740753248740754AG27GENIChomozygous110372478
2248741125248741126AG29GENIChomozygous110372480
2248742740248742741CG18GENIChomozygous110372482
2248743971248743972TC29GENIChomozygous110372484
2248744152248744153CT25GENIChomozygous110372486
2248744156248744157CA25GENIChomozygous110372488
2248745750248745751TC16GENIChomozygous110372490
2248749345248749346TC19GENIChomozygous110372495
2248753476248753477TC18GENIChomozygous110372497
2248755338248755339CA29GENIChomozygous110372499
2248765341248765342GT31GENIChomozygous110372501
2248771089248771090CT26GENIChomozygous110372503
2248775944248775945GA35GENIChomozygous110372505
2248777397248777398CT27GENIChomozygous110372507
2248781961248781962GA19GENIChomozygous110372509
2248793771248793772AC36GENIChomozygous110372511
2248797781248797782CA29GENIChomozygous110372513
2248799837248799838GA40GENIChomozygous110372515
2248813755248813756GA21GENIChomozygous110372525
2248815685248815686TA22GENIChomozygous110372527
2248818866248818867CT28GENICpossibly homozygous110372529
2248820139248820140AG20GENIChomozygous110372531
2248821616248821617TC27GENIChomozygous110372533
2248831507248831508AG18GENIChomozygous110372535
2248835795248835796TC23GENIChomozygous110372537