chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124189419541894196T-13GENICheterozygous926984957
124189472641894727CCAGCT17GENICheterozygous926984958
124189682141896822TC16GENICheterozygous926855019
124192817841928179CG21GENICheterozygous926855020
124193411941934120GA12GENICheterozygous926855021
124193828041938281TC6GENICheterozygous926855022
124194877241948773AG5GENICheterozygous926855023
124195921341959214CA26GENICheterozygous926855024
124196791741967918AT28GENICheterozygous926855025
124198878141988782CT25GENICheterozygous926855026
124199137341991374AG45GENICheterozygous926855027
124199137441991375AC44GENICheterozygous926855028
124199140441991405AC32GENICheterozygous926855029
124199157641991578AA--13GENICheterozygous926984959
124200333642003337TC13GENICheterozygous926855030
124200400742004008AT47GENICheterozygous926855031
124201654642016547G-12GENICheterozygous926984960
124201704442017045AC6GENICheterozygous926855032
124201730742017308AG79GENICheterozygous926855033
124201737842017379AG48GENICheterozygous926855034
124201949942019500AG12GENICheterozygous926855035
124203211042032111TC8GENICheterozygous926855036
124203727642037277TC13GENICheterozygous926855037
124203731442037315AG15GENICheterozygous926855038
124203734042037341TC15GENICheterozygous926855039
124203740042037402GG--17GENICheterozygous926984961
124203740242037403GA17GENICheterozygous926855040
124203741042037411GA13GENICheterozygous926855041
124203741142037412GA13GENICheterozygous926855042
124203742142037422GA13GENICheterozygous926855043
124203743542037436AT15GENICheterozygous926855044
124203766142037662AG6GENICheterozygous926855045
124206018842060189GA11GENICheterozygous926855046
124206528942065290GA6GENICheterozygous926855047
124207166842071669TC38GENICheterozygous926855048
124207314442073145GA26GENICheterozygous926855049
124207633442076335GA9GENICheterozygous926855050
124208317842083179AC9GENICheterozygous926855051
124209007742090078TC27GENICheterozygous926855052