chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7120387249120387250GA36GENIChomozygous54084081
7120387941120387942TC37GENIChomozygous54084082
7120388694120388695AG41GENIChomozygous54084083
7120389509120389510CT23GENIChomozygous54084084
7120389607120389608AG27GENIChomozygous54084085
7120389713120389714AG16GENIChomozygous54084086
7120390296120390297AG31GENIChomozygous54084087
7120390388120390389GC28GENIChomozygous54084089
7120390517120390518CT21GENIChomozygous54859819
7120390852120390853CT30GENIChomozygous54084090
7120390927120390928TC25GENIChomozygous54084091
7120391170120391171AG26GENIChomozygous54084092
7120391780120391781AG22GENIChomozygous54084093
7120392222120392223GA26GENIChomozygous54084094
7120392714120392715CT33GENIChomozygous54084095
7120393276120393277GA30GENIChomozygous54859820
7120393749120393750TC23GENIChomozygous54084096
7120394682120394683AACAGCTAGAC27GENIChomozygous54084097
7120394797120394798TC23GENIChomozygous54084098
7120394923120394924TC4GENIChomozygous54084099
7120394944120394945TG2GENIChomozygous54084100
7120395441120395442TC15GENIChomozygous54084101
7120395938120395939GGGTTTTTTT5GENICheterozygous55030408
7120395946120395947TTG6GENICheterozygous54084102
7120395961120395962TTG6GENICheterozygous55001602