chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
37755217277552173AC32GENIChomozygous57473701
37755246377552464G-15GENICheterozygous57473703
37755282577552826AG30GENIChomozygous57473705
37755286477552865CG27GENIChomozygous57473707
37755310477553105AG24GENIChomozygous57473709
37755347877553479CT21GENIChomozygous57473712
37755391777553918G-22GENIChomozygous57473714
37755467277554673CT31GENIChomozygous57473716
37755717277557173GA22GENIChomozygous57473718
37755796177557962A-18GENICpossibly homozygous57473720
37756013477560135GA31GENIChomozygous57473722
37756058777560588AT14GENIChomozygous57473724
37756105977561060GA33GENIChomozygous57473726
37756156277561563TA24GENIChomozygous57473728
37756163877561639CA30GENIChomozygous57473730
37756240977562410TG44GENIChomozygous57473732
37756310277563103T-8GENIChomozygous57473734
37756310277563103TTAA13GENIChomozygous57473736
37756390077563901GA40GENIChomozygous57473738
37756444977564450GA23GENIChomozygous57473740
37756471577564716T-23GENIChomozygous57473742
37756494977564951TT--14GENICpossibly homozygous57473746
37756495077564951T-14GENICheterozygous58157691
37756499077564991GA23GENIChomozygous57473748
37756569877565699GGA15GENIChomozygous57473750
37756570577565706GGTGT16GENIChomozygous57473752
37756607077566071TG19GENICheterozygous57473754
37756730477567305C-42GENIChomozygous57473756
37756772577567726GT15GENIChomozygous57473758
37756855977568560AAAGGGTTACTGGAAT16GENIChomozygous57473760
37756857577568576AG17GENICheterozygous57473762
37756867777568680GGG---14GENIChomozygous57473764
37756883477568835AG26GENIChomozygous57473766
37756965177569654TTG---22GENIChomozygous57473768