chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
181527229515272296TG18GENIChomozygous110281698
181527244915272450AG20GENIChomozygous110281700
181527245215272453CT19GENIChomozygous110452492
181527334015273341GT9GENIChomozygous110281702
181527362315273624AG27GENIChomozygous110452493
181527375815273759TC19GENIChomozygous110281706
181527376315273764AC19GENIChomozygous110281708
181527418015274181GC18GENIChomozygous110281712
181527420315274204AT20GENIChomozygous110281714
181527432315274324GA19GENIChomozygous110452494
181527445815274459GA8GENIChomozygous110281716
181527485915274860GT20GENIChomozygous110452495
181527639315276394CT11GENIChomozygous110452496
181527639515276396TC11GENIChomozygous110452497
181527652915276530CT21GENIChomozygous110452498
181527665615276657CA24GENIChomozygous110525373
181527674415276745CA23GENIChomozygous110452499
181527679115276792TC14GENIChomozygous110452500
181527712215277123TC24GENIChomozygous110452501
181527717515277176GA19GENIChomozygous110452502
181527718815277189GC24GENIChomozygous110452503
181527771915277720AC18GENIChomozygous110452504
181527780315277804GA29GENIChomozygous110452505
181527784115277842TG19GENIChomozygous110452506
181527791515277916GA23GENIChomozygous110452507
181527802715278028GA11GENIChomozygous110452508
181527983415279835TC21GENIChomozygous110281720
181527999015279991GA30GENIChomozygous110452510
181528021315280214TC31GENIChomozygous110452511
181528109215281093TC9GENIChomozygous110452512
181528159015281591GC29GENIChomozygous110452513
181528165315281654AG18GENIChomozygous110452514
181528192015281921GA11GENIChomozygous110452515
181528215115282152AG11GENIChomozygous110452516
181527588315275884TC5GENIChomozygous110885754