chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5147721535147721542ACAAATT36GENIChomozygous128253898
5147722337147722338AT34GENIChomozygous114153090
5147722571147722571G7GENICheterozygous128253900
5147723343147723344GA48GENIChomozygous114047016
5147723732147723733AT52GENIChomozygous114047018
5147724691147724692GA37GENIChomozygous114047024
5147724869147724869TTTCTTTC30GENIChomozygous128253901
5147726247147726248GA35GENIChomozygous114047026
5147727067147727068TC41GENICpossibly homozygous114047028
5147727364147727365CT11GENIChomozygous114047030
5147727669147727670CG28GENIChomozygous114047032
5147728259147728260AG26GENIChomozygous114047034
5147728918147728919AG41GENIChomozygous114047036
5147729096147729096AACTCAGTTGGTCT42GENIChomozygous128253902
5147729548147729548T33GENIChomozygous128253903
5147732002147732002G46GENIChomozygous128253904
5147733074147733075CT49GENIChomozygous114047038
5147734121147734122TC49GENIChomozygous114047040
5147734239147734240T51GENIChomozygous128253905
5147734261147734262GA53GENIChomozygous114047042
5147735322147735323TC56GENIChomozygous114047044
5147736065147736066A25GENICheterozygous128253907
5147736582147736583AT47GENIChomozygous114047046
5147736835147736866TTTTGTCTTTTTTTTTTTTTTTTTTTTTTTT44GENIChomozygous128253908
5147738756147738757TA43GENIChomozygous114047050
5147739705147739705AAC20GENIChomozygous128253909
5147740877147740878AG48GENIChomozygous114047052
5147740993147740994AC39GENIChomozygous114047054
5147741744147741745TG36GENIChomozygous114047058
5147741811147741811T34GENIChomozygous128253910
5147741912147741913GA40GENIChomozygous114047060
5147742079147742080G31GENIChomozygous128253912
5147742438147742439GA28GENIChomozygous114047062
5147742484147742485CA15GENIChomozygous114047064
5147743184147743185TC44GENIChomozygous114153093
5147741827147741827AT27GENICpossibly homozygous132079726