chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
166445623264456233CT9GENICheterozygous47485250
166445638764456388AC9GENICpossibly homozygous47818966
166445649064456491TC12GENIChomozygous47818968
166445706464457065AAACACACACACACACACACACACACACACAC2GENIChomozygous47908582
166445726564457266AG17GENICpossibly homozygous47818972
166445730964457310CT16GENIChomozygous47818974
166445763164457634GAG---1GENIChomozygous47818976
166445787264457873CCTAGCAGATATCT1GENIChomozygous47485251
166445870464458705TC17GENICpossibly homozygous47485252
166445885164458852GT4GENIChomozygous47485253
166445920764459208GA26GENICpossibly homozygous47485254
166445936264459363TC34GENICpossibly homozygous47485255
166445946264459463AG16GENICheterozygous47485256
166445958164459582CA14GENICpossibly homozygous47818978
166445991964459920CT29GENICpossibly homozygous47818980
166446005564460056C-6GENIChomozygous47485259
166446008464460085C-7GENICheterozygous47684858
166446008464460085CA7GENICpossibly homozygous47908583
166446022564460226GT16GENICheterozygous47485261
166446030564460306CT19GENICpossibly homozygous47485262
166446036264460363AC17GENIChomozygous47818982
166446184564461846TC15GENICpossibly homozygous47485264