chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104706760647067607GA13GENIChomozygous887194982
104706797347067974AC18GENIChomozygous887194983
104708175547081756TG21GENIChomozygous887194984
104708237347082374GA10GENIChomozygous887194985
104708241747082418AC7GENIChomozygous887194986
104708255747082558GA17GENIChomozygous887194987
104708275547082756TG11GENIChomozygous887194988
104708308147083082GA16GENIChomozygous887194989
104708432247084323AG9GENIChomozygous887194990
104708446147084462TC23GENIChomozygous887194991
104708582047085821CT20GENIChomozygous887194992
104708587347085874TC15GENIChomozygous887194993
104708642247086423GC23GENIChomozygous887194994
104708650047086501AG19GENIChomozygous887194995
104708734847087349GA20GENIChomozygous887194996
104708819347088194GT24GENIChomozygous887194997
104708985847089859GA8GENIChomozygous887194998
104708996147089962TC18GENIChomozygous887194999
104709048247090483TC23GENIChomozygous887195000
104709050647090507GT28GENIChomozygous887195001
104709079447090795CA19GENIChomozygous887195002
104709128847091289GT21GENIChomozygous887195003
104709153347091534CT11GENIChomozygous887195004
104709154247091543CT10GENIChomozygous887195005
104709168447091685GA11GENIChomozygous887195006
104709189647091897CT23GENIChomozygous887195007
104709296347092964TC23GENIChomozygous887195008
104709340447093405TC21GENIChomozygous887195009
104709370847093709TG19GENIChomozygous887195010
104709401947094020TC14GENIChomozygous887195011
104709471147094712TC11GENICheterozygous887195012
104709540047095401AC29GENIChomozygous887195013
104709700447097005TC24GENIChomozygous887195014
104710045347100454CT29GENIChomozygous887195015
104710175847101759CT14GENIChomozygous887195016
104710532847105329TC17GENIChomozygous887195017
104710603047106031TC5GENIChomozygous887195018
104710799847107999AG29GENIChomozygous887195019
104710810447108105CG26GENIChomozygous887195020