chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
193093700030937001GA22GENIChomozygous109805770
193093862330938624GT10GENIChomozygous109805772
193093941630939419GAT22GENIChomozygous129600657
193093962330939624TA11GENIChomozygous109805775
193093966630939667TA4GENIChomozygous109805777
193093973530939736AG3GENIChomozygous109679067
193094046130940462A21GENIChomozygous129600658
193094053830940539TC15GENIChomozygous109805779
193094230130942302GA16GENIChomozygous109679071
193094397330943974GA25GENIChomozygous109679073
193094585330945854AG13GENIChomozygous109679075
193094685030946851AT14GENIChomozygous109679079
193094752130947522CT21GENIChomozygous109679081
193094752130947521G22GENIChomozygous129600660
193095043130950432GA13GENIChomozygous109679085
193095163130951632TC21GENIChomozygous109805781
193095250030952500A14GENIChomozygous129600662
193095342630953427GA20GENICpossibly homozygous109805783
193095404630954047CT18GENIChomozygous109679087
193095539330955394GA16GENIChomozygous109805785
193095645530956455GGCATGTTATATGC14GENIChomozygous129600664
193095834630958347AG20GENIChomozygous109679095
193095911930959120TC13GENIChomozygous109679097
193096058830960589T15GENICpossibly homozygous129600665
193096140230961402T17GENICheterozygous130799541
193096142730961428GT17GENIChomozygous109679101
193096430130964302CT17GENIChomozygous109805787
193096663830966639GT10GENIChomozygous109805789
193096665430966655T10GENIChomozygous129600666
193096702630967030TAGA11GENIChomozygous132233883
193095376030953767AAAAAAG6GENIChomozygous132233880
193096125630961256T14GENIChomozygous132233881
193096189830961900TT12GENIChomozygous132233882
193096131330961314GT12GENIChomozygous109919070
193096132030961321GT13GENIChomozygous109919072
193096743930967440AG18GENIChomozygous109679109
193096782030967821GA20GENIChomozygous109919074
193096916230969163T16GENIChomozygous129600668