chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5147720197147720198A56GENICheterozygous128253897
5147721535147721542ACAAATT58GENIChomozygous128253898
5147722337147722338AT70GENIChomozygous114153090
5147722571147722571G9GENIChomozygous128253900
5147723343147723344GA66GENIChomozygous114047016
5147723732147723733AT84GENIChomozygous114047018
5147724691147724692GA59GENIChomozygous114047024
5147724869147724869TTTCTTTC42GENICpossibly homozygous128253901
5147726247147726248GA58GENIChomozygous114047026
5147727067147727068TC42GENIChomozygous114047028
5147727364147727365CT18GENICpossibly homozygous114047030
5147727669147727670CG41GENIChomozygous114047032
5147728259147728260AG29GENIChomozygous114047034
5147728918147728919AG51GENIChomozygous114047036
5147729096147729096AACTCAGTTGGTCT55GENIChomozygous128253902
5147729548147729548T44GENICpossibly homozygous128253903
5147732002147732002G53GENIChomozygous128253904
5147733074147733075CT63GENIChomozygous114047038
5147734121147734122TC49GENIChomozygous114047040
5147734239147734240T40GENIChomozygous128253905
5147734261147734262GA44GENIChomozygous114047042
5147734690147734699GTTTTTTTG14GENICheterozygous128253906
5147735322147735323TC54GENIChomozygous114047044
5147736582147736583AT58GENIChomozygous114047046
5147736835147736866TTTTGTCTTTTTTTTTTTTTTTTTTTTTTTT36GENIChomozygous128253908
5147738756147738757TA63GENIChomozygous114047050
5147739705147739705AAC37GENIChomozygous128253909
5147740877147740878AG54GENIChomozygous114047052
5147740993147740994AC58GENIChomozygous114047054
5147741744147741745TG61GENIChomozygous114047058
5147741811147741811T49GENIChomozygous128253910
5147741912147741913GA54GENIChomozygous114047060
5147742438147742439GA46GENIChomozygous114047062
5147742484147742485CA23GENIChomozygous114047064
5147743184147743185TC43GENIChomozygous114153093
5147741827147741827AT43GENICpossibly homozygous132079726
5147742079147742080G43GENIChomozygous128253912