chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
134712717447127178TCTG----15GENIChomozygous49751035
134712868347128685TT--14GENICheterozygous50357802
134713119347131197GTGT----17GENIChomozygous49751036
134713202147132022GGGT20GENICheterozygous49751037
134713327647133277CG29GENICpossibly homozygous49751040
134713528947135290GA24GENICheterozygous49751041
134713529147135292CA22GENICheterozygous49751042
134713641247136413TG23GENIChomozygous49751043
134714336447143365AAGT24GENIChomozygous49751044
134714346947143470AT38GENIChomozygous49751045
134714490347144905TG--19GENIChomozygous49751046
134714528947145290GGCA16GENICheterozygous49751047
134714529047145292CA--16GENICheterozygous49751048
134714634947146350CT20GENIChomozygous49751049
134714802447148025TTACACACAC25GENICheterozygous50357804
134714827247148273TTAC11GENICheterozygous49751050
134714827247148273TTACAC11GENICheterozygous49751051
134714850447148505GC29GENIChomozygous49751052
134714852347148524TA30GENIChomozygous49751053
134714870747148708GA31GENIChomozygous49751054
134714888647148887G-22GENIChomozygous49751055
134714921547149216TC18GENIChomozygous49751056
134714923147149232GA14GENIChomozygous49751057
134714965947149660AG17GENIChomozygous49751058