chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2203922569203922570CA27GENIChomozygous142981824
2203922930203922931CA21GENIChomozygous142981825
2203925851203925852GC19GENIChomozygous142981826
2203926812203926813GA18GENIChomozygous142981827
2203927068203927069AG23GENIChomozygous142981828
2203930070203930071CT16GENIChomozygous142981829
2203931469203931470TC19GENIChomozygous142981830
2203932269203932270TC16GENIChomozygous136446038
2203932763203932764CT16GENIChomozygous142981831
2203933649203933650CA18GENIChomozygous136446040
2203933824203933825GA27GENIChomozygous142981832
2203934586203934587GA16GENIChomozygous142981833
2203934621203934621T13GENIChomozygous142904516
2203930981203930981TGTATT18GENIChomozygous142904513
2203931658203931659C16GENIChomozygous142904514
2203933720203933720A21GENIChomozygous142904515
2203935453203935454CG16GENIChomozygous142981834
2203935801203935802GA10GENIChomozygous136446043
2203935948203935949CT26GENIChomozygous142981835
2203939530203939531AG23GENIChomozygous136446045
2203940241203940242CT16GENIChomozygous142981836
2203941125203941150TTTCTTTCTTTCTTTCTTTCTTTCT14GENIChomozygous142904517
2203941716203941717GA23GENIChomozygous142981837
2203943120203943121T20GENIChomozygous142904518
2203944048203944049TC14GENIChomozygous136446048
2203946043203946044TG10GENIChomozygous142981838