chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
193093941630939419GAT34GENIChomozygous129600657
193093973530939736AG15GENIChomozygous109679067
193094019430940195CA44GENIChomozygous109679069
193094046130940462A40GENIChomozygous129600658
193094099930941001GG17GENIChomozygous129600659
193094230130942302GA52GENIChomozygous109679071
193094397330943974GA42GENIChomozygous109679073
193094585330945854AG51GENIChomozygous109679075
193094610730946108GA48GENIChomozygous109679077
193094685030946851AT45GENIChomozygous109679079
193094752130947522CT56GENIChomozygous109679081
193094752130947521G56GENIChomozygous129600660
193094851730948518GA42GENIChomozygous109679083
193094967330949690AATGTAGGTAAAGCACG52GENIChomozygous129600661
193095043130950432GA53GENIChomozygous109679085
193095091430950915TG18GENICheterozygous130715870
193095163130951632TC50GENIChomozygous109805781
193095250030952500A47GENIChomozygous129600662
193095404630954047CT37GENIChomozygous109679087
193095428830954289GT39GENIChomozygous109679089
193095532830955329A28GENICpossibly homozygous129600663
193095539030955391GA44GENIChomozygous109679091
193095626630956267CT47GENIChomozygous109679093
193095645530956455GGCATGTTATATGC44GENIChomozygous129600664
193095834630958347AG38GENIChomozygous109679095
193095911930959120TC51GENIChomozygous109679097
193096058830960589T34GENIChomozygous129600665
193096133830961339CT37GENIChomozygous119624172
193096098430960985TA40GENIChomozygous109679099
193096142730961428GT42GENIChomozygous109679101
193096154730961548GC50GENIChomozygous109679103
193096131330961314GT30GENIChomozygous109919070
193096132030961321GT28GENIChomozygous109919072
193096383130963832GA39GENIChomozygous109679105
193096665430966655T44GENIChomozygous129600666
193096739930967400GA50GENIChomozygous109679107
193096743930967440AG54GENIChomozygous109679109
193096782030967821GA35GENIChomozygous109919074
193096817430968175GA38GENIChomozygous109679111
193096906730969067T52GENICpossibly homozygous129600667
193096916230969163T45GENIChomozygous129600668