chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
18255165582551656CG25GENIChomozygous120779939
18255169182551692TC24GENIChomozygous120481982
18255169782551698AT22GENIChomozygous120481983
18255174782551748AG28GENIChomozygous120779940
18255209182552092GC30GENIChomozygous120481984
18255223382552234CT31GENIChomozygous120779941
18255246082552461TC30GENIChomozygous120481985
18255359182553592CA22GENIChomozygous120779942
18255384882553849GA29GENIChomozygous120779943
18255385582553856CT31GENIChomozygous120779944
18255387282553873GA32GENIChomozygous120779945
18255406482554065GT30GENIChomozygous120481986
18255467282554673AG28GENIChomozygous120481987
18255485982554860AG30GENICpossibly homozygous120481988
18255488982554890AT30GENIChomozygous108878254
18255625882556259TC13GENIChomozygous120779946
18255666582556666TG41GENIChomozygous108878255
18255803482558035CT25GENIChomozygous108878256
18255855982558560GA52GENIChomozygous120481990
18255869482558695CA39GENIChomozygous120481991
18255923182559232GA19GENIChomozygous120779947
18255953982559540AG14GENIChomozygous108878258
18255960882559609GA18GENIChomozygous120779948
18255966782559668TC13GENIChomozygous120481992
18256008782560088CA17GENIChomozygous120779949
18256081882560819TC38GENIChomozygous120481995
18256126482561265TG11GENIChomozygous108729123
18256126582561266GT11GENIChomozygous120472168
18256276182562762GA13GENIChomozygous108140554
18256278682562787TG10GENIChomozygous108729125
18256278782562788AT10GENIChomozygous108729126
18256295282562953GA13GENIChomozygous108878259
18256416982564170AG28GENIChomozygous120779950
18256449882564499CG9GENIChomozygous108878262
18257025882570259CT34GENIChomozygous120779951
18257748982577490CT27GENIChomozygous120779952
18257895182578952CT9GENIChomozygous108878269