chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X4697896546978966GT5GENIChomozygous787841957
X4698047346980474GA9GENIChomozygous787841958
X4699030346990304CT5GENIChomozygous787841959
X4699037246990373GT8GENIChomozygous787841960
X4699041646990417TG8GENIChomozygous787841961
X4699050846990509AC5GENIChomozygous787841962
X4699252146992522CT10GENICheterozygous787841963
X4699256546992566TC10GENICheterozygous787841964
X4699293446992935AG20GENIChomozygous787841965
X4699539946995400AC13GENIChomozygous787841966
X4699556346995564CT13GENIChomozygous787841967
X4699656146996562TC11GENICheterozygous787841968
X4699661846996619GA7GENIChomozygous787841969
X4700354147003542TA7GENIChomozygous787841970
X4700358147003582CT3GENIChomozygous787841971
X4700365247003653CA5GENIChomozygous787841972
X4700380447003805CA2GENIChomozygous787841973
X4700435447004355CT10GENIChomozygous787841974
X4700842547008426GA10GENIChomozygous787841975
X4700873947008740GA7GENIChomozygous787841976
X4700983947009840AG16GENIChomozygous787841977
X4701146647011467AG11GENIChomozygous787841978
X4701181447011815CT14GENIChomozygous787841979
X4701302747013028CT13GENIChomozygous787841980
X4701486347014864AC15GENIChomozygous787841981
X4701660847016609AG6GENIChomozygous787841982
X4701675447016755TA5GENIChomozygous787841983
X4702029747020298TC5GENIChomozygous787841984
X4702521947025220CT12GENIChomozygous787841985
X4702589247025893TC12GENIChomozygous787841986