chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
193093941630939419GAT52GENIChomozygous129600657
193093973530939736AG11GENIChomozygous109679067
193094019430940195CA57GENIChomozygous109679069
193094046130940462A49GENIChomozygous129600658
193094099930941001GG34GENIChomozygous129600659
193094230130942302GA58GENIChomozygous109679071
193094397330943974GA55GENIChomozygous109679073
193094585330945854AG54GENIChomozygous109679075
193094610730946108GA59GENIChomozygous109679077
193094685030946851AT57GENIChomozygous109679079
193094752130947522CT63GENIChomozygous109679081
193094752130947521G62GENIChomozygous129600660
193094851730948518GA73GENIChomozygous109679083
193094967330949690AATGTAGGTAAAGCACG67GENIChomozygous129600661
193095043130950432GA73GENIChomozygous109679085
193095163130951632TC63GENIChomozygous109805781
193095250030952500A56GENIChomozygous129600662
193095404630954047CT46GENIChomozygous109679087
193095428830954289GT43GENIChomozygous109679089
193095532830955329A45GENICpossibly homozygous129600663
193095539030955391GA52GENIChomozygous109679091
193095626630956267CT61GENIChomozygous109679093
193095645530956455GGCATGTTATATGC51GENIChomozygous129600664
193095834630958347AG65GENIChomozygous109679095
193095911930959120TC39GENIChomozygous109679097
193096058830960589T47GENICpossibly homozygous129600665
193096098430960985TA37GENICpossibly homozygous109679099
193096131330961314GT38GENIChomozygous109919070
193096132030961321GT37GENIChomozygous109919072
193096133830961339CT36GENIChomozygous119624172
193096142730961428GT44GENIChomozygous109679101
193096154730961548GC47GENIChomozygous109679103
193096383130963832GA47GENIChomozygous109679105
193096665430966655T44GENIChomozygous129600666
193096739930967400GA39GENIChomozygous109679107
193096743930967440AG49GENIChomozygous109679109
193096782030967821GA43GENIChomozygous109919074
193096817430968175GA59GENICpossibly homozygous109679111
193096906730969067T53GENICpossibly homozygous129600667
193096916230969163T51GENIChomozygous129600668