chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
79962624799626248AG16GENIChomozygous889697978
79962932399629324CG13GENIChomozygous889697979
79963048599630486AC23GENIChomozygous889697980
79963077699630777GA27GENIChomozygous889697981
79963276699632767CT19GENIChomozygous889697982
79963354999633550CG13GENIChomozygous889697983
79963494799634948TC23GENIChomozygous889697984
79963561799635618CT18GENIChomozygous889697985
79963574199635742CG21GENIChomozygous889697986
79963580699635807TC20GENIChomozygous889697987
79963718599637186CT17GENIChomozygous889697988
79963932799639328AG15GENIChomozygous889697989
79963952299639523CG4GENIChomozygous889697990
79963999099639991AT8GENIChomozygous889697991
79964003299640033TA11GENICheterozygous889697992
79964114399641144CA32GENIChomozygous889697993
79964581299645813AT15GENIChomozygous889697994
79965331599653316AG30GENIChomozygous889697995
79965548599655486AG12GENIChomozygous889697996
79965804199658042CT17GENIChomozygous889697997
79965822799658228CT27GENIChomozygous889697998
79965867699658677CT20GENIChomozygous889697999
79967021699670217AC19GENIChomozygous889698000
79967094699670947TC14GENICheterozygous889698001
79967147199671472TC20GENIChomozygous889698002
79967227699672277CT16GENIChomozygous889698003
79967241699672417GA24GENIChomozygous889698004
79967301499673015CT30GENIChomozygous889698005
79967466099674661AC11GENICheterozygous889698006
79967477899674779AC9GENICheterozygous889698007
79967486299674863CA15GENICheterozygous889698008
79967489099674891TG16GENIChomozygous889698009
79967499299674993AG7GENICheterozygous889698010
79967523299675233CG21GENICheterozygous889698011
79967527799675278TC23GENICheterozygous889698012
79967533699675337GA23GENICheterozygous889698013
79967552999675530AT9GENIChomozygous889698014
79967648799676488TC23GENIChomozygous889698015