chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
181527212615272127CT17GENIChomozygous110525365
181527229515272296TG22GENIChomozygous110281698
181527244915272450AG18GENIChomozygous110281700
181527245215272453CT19GENIChomozygous110452492
181527334015273341GT15GENIChomozygous110281702
181527362315273624AG30GENIChomozygous110452493
181527375815273759TC35GENIChomozygous110281706
181527418015274181GC25GENIChomozygous110281712
181527420315274204AT24GENIChomozygous110281714
181527432315274324GA22GENIChomozygous110452494
181527485915274860GT11GENIChomozygous110452495
181527534215275343CT14GENIChomozygous110525367
181527537015275371TG11GENIChomozygous110525369
181527639315276394CT19GENIChomozygous110452496
181527639515276396TC17GENIChomozygous110452497
181527652915276530CT15GENIChomozygous110452498
181527665615276657CA19GENIChomozygous110525373
181527674415276745CA23GENIChomozygous110452499
181527679115276792TC26GENIChomozygous110452500
181527709215277093TC25GENIChomozygous110525375
181527712215277123TC25GENIChomozygous110452501
181527717515277176GA24GENIChomozygous110452502
181527728815277289CG15GENICpossibly homozygous110702083
181527771915277720AC21GENIChomozygous110452504
181527780315277804GA29GENIChomozygous110452505
181527784115277842TG29GENIChomozygous110452506
181527791515277916GA24GENIChomozygous110452507
181527802715278028GA21GENIChomozygous110452508
181527866415278665CT11GENIChomozygous110452509
181527983415279835TC36GENIChomozygous110281720
181527999015279991GA33GENIChomozygous110452510
181528021315280214TC25GENIChomozygous110452511
181528109215281093TC11GENIChomozygous110452512
181528159015281591GC24GENIChomozygous110452513
181528165315281654AG17GENIChomozygous110452514
181528178015281781AG18GENIChomozygous110525379
181528192015281921GA26GENIChomozygous110452515
181527867315278674GA12GENIChomozygous110712767
181527264015272641CT7GENIChomozygous110722768
181527267215272673CT2GENIChomozygous110722770