chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
17169968671699687CT18GENIChomozygous109105008
17170221571702216AG17GENIChomozygous109105010
17170222771702228AG15GENIChomozygous108864033
17170230471702305CT25GENIChomozygous109105012
17170234971702350AC16GENIChomozygous108864034
17170250371702504AG9GENIChomozygous109105014
17170267871702679CG11GENIChomozygous108864035
17170269071702691CA6GENIChomozygous108864036
17170269871702699GA7GENIChomozygous108864037
17170379771703798CT14GENIChomozygous108727602
17170382871703829AT9GENICheterozygous108132682
17170389971703900TC23GENIChomozygous108864043
17170416571704166AT29GENIChomozygous108864044
17170434471704345AG17GENIChomozygous108864045
17170444971704450GA18GENIChomozygous108864046
17170459271704593CT13GENIChomozygous109105016
17170476571704766GA8GENIChomozygous109105018
17170481671704817CT12GENIChomozygous108864047
17170499671704997CA21GENIChomozygous108864048
17170522371705224CA5GENIChomozygous120480900
17170575971705760TC15GENIChomozygous108864052
17170578271705783GC16GENIChomozygous108864053
17170582571705826AG10GENIChomozygous108864054
17170588971705890CT7GENIChomozygous108864055
17170609471706095CA11GENIChomozygous109105020
17170616771706168GT20GENICpossibly homozygous108864056
17170618071706181GA17GENIChomozygous108864057
17170677571706776CA12GENIChomozygous109105022
17170767571707676AT17GENIChomozygous109105024
17170791471707915CA13GENIChomozygous109105026
17170835271708353CG4GENICheterozygous125426917
17170883571708836AG12GENIChomozygous108864064
17170920671709207TC16GENIChomozygous108864065
17170951171709512GC24GENIChomozygous108864066
17171050971710510AT14GENIChomozygous109105028
17171059171710592AC14GENIChomozygous109105030
17171320171713202TC20GENIChomozygous108864068
17171425371714254TC10GENIChomozygous109105040
17171435971714360GT24GENIChomozygous109105041
17171439271714393TA13GENIChomozygous108864069
17171450371714504CT21GENIChomozygous109105043