chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
63609097436090975TA45GENIChomozygous115103795
63609260536092606T31GENIChomozygous132092198
63609501436095015AG36GENIChomozygous115103796
63609515736095158CG46GENIChomozygous115103797
63609547536095475A40GENIChomozygous132092199
63609703936097040GA39GENIChomozygous115103798
63609794536097946GT40GENIChomozygous115103799
63610103236101032G21GENIChomozygous128329511
63609524036095241G42GENIChomozygous130325964
63610094536100945A19GENIChomozygous128329508
63610098536100985GG24GENIChomozygous128329509
63610098936100990A24GENIChomozygous128329510
63610108336101084C32GENIChomozygous132092201
63610112136101121T29GENIChomozygous128329512
63610113536101135T24GENIChomozygous128329513
63610117836101178T19GENIChomozygous128329514
63610251936102520CT49GENIChomozygous115103800
63610282536102826CA46GENIChomozygous115103801
63610282636102827GA45GENIChomozygous115103802
63610288236102883CT45GENIChomozygous115103803
63610289036102891GA45GENIChomozygous115103804
63610364036103641AG48GENIChomozygous115103805
63610396136103962CT51GENIChomozygous115103806
63610400436104005TC48GENIChomozygous115103807
63610400536104006GA48GENIChomozygous115103808
63610533636105337AT42GENIChomozygous115103809
63610163336101634T42GENICpossibly homozygous131407316