chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
37755217277552173AC21GENIChomozygous57473701
37755282577552826AG20GENIChomozygous57473705
37755286477552865CG19GENIChomozygous57473707
37755310477553105AG16GENIChomozygous57473709
37755347877553479CT26GENIChomozygous57473712
37755391777553918G-20GENIChomozygous57473714
37755467277554673CT22GENIChomozygous57473716
37755587977555880GA18GENIChomozygous58531686
37755717277557173GA18GENIChomozygous57473718
37755796177557962A-17GENIChomozygous57473720
37755796977557970A-19GENICheterozygous57904142
37756013477560135GA18GENIChomozygous57473722
37756058777560588AT2GENIChomozygous57473724
37756105977561060GA18GENIChomozygous57473726
37756156277561563TA18GENIChomozygous57473728
37756163877561639CA23GENIChomozygous57473730
37756240977562410TG13GENIChomozygous57473732
37756310377563104TA8GENIChomozygous58550990
37756390077563901GA11GENIChomozygous57473738
37756444977564450GA22GENIChomozygous57473740
37756471577564716T-16GENICpossibly homozygous57473742
37756499077564991GA15GENIChomozygous57473748
37756569877565699GGA17GENIChomozygous57473750
37756570577565706GGTGT14GENIChomozygous57473752
37756730477567305C-23GENIChomozygous57473756
37756772577567726GT11GENIChomozygous57473758
37756855977568560AAAGGGTTACTGGAAT14GENIChomozygous57473760
37756867777568680GGG---18GENIChomozygous57473764
37756883477568835AG22GENIChomozygous57473766
37756965177569654TTG---18GENIChomozygous57473768
37756310277563103TTA8GENIChomozygous58597464
37756494877564950TT--12GENIChomozygous58597466