chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
62236792422367925GA31GENIChomozygous118729981
62236946922369470GT16GENIChomozygous114738057
62237031422370315TC24GENIChomozygous114738060
62237239022372391TC25GENIChomozygous114738061
62237242122372422GA26GENIChomozygous118729982
62237256022372561TG22GENIChomozygous118729983
62237270322372704GA20GENIChomozygous114738062
62237507422375075AG13GENIChomozygous118729984
62237531122375312CG20GENIChomozygous114738067
62237595422375955AG12GENIChomozygous114738069
62237626622376267AT16GENIChomozygous114738070
62237762622377627GA19GENIChomozygous118729985
62237812522378126TA12GENIChomozygous114738072
62237988822379889AG22GENIChomozygous114738074
62238018122380182AG20GENIChomozygous114738075
62238493322384934GA31GENIChomozygous118729986
62238548722385488GA23GENIChomozygous118729987
62238694622386947GA18GENIChomozygous118729988
62238839322388394AC11GENIChomozygous118729989
62238865922388660TA30GENIChomozygous114738079
62238878422388785AG12GENIChomozygous114738080
62238994622389947TA12GENIChomozygous118729990
62238996722389968CA13GENIChomozygous118729991
62239165122391652GA35GENIChomozygous114738084
62239249022392491TC23GENIChomozygous114738086
62239269822392699CT22GENIChomozygous118729992
62239300922393010CT20GENIChomozygous114738087
62239309722393098GA34GENIChomozygous118729993
62239457922394580GA29GENIChomozygous114738090
62239513922395140GA32GENIChomozygous118729994
62239639622396397TC43GENIChomozygous114738092
62239717222397173CT30GENIChomozygous114738094
62239750022397501CT23GENICpossibly homozygous118729995
62240056322400564CA15GENIChomozygous118729996
62240236222402363GC31GENIChomozygous118729997
62240300822403009AT28GENIChomozygous118729998
62240318922403190TC29GENIChomozygous118729999
62240351122403512TA23GENIChomozygous114738100
62240588022405881TC23GENIChomozygous114738103
62240618122406182TA32GENIChomozygous114738105