chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7120387249120387250GA43GENIChomozygous54084081
7120387941120387942TC45GENIChomozygous54084082
7120388694120388695AG59GENIChomozygous54084083
7120389509120389510CT48GENIChomozygous54084084
7120389607120389608AG63GENIChomozygous54084085
7120389713120389714AG42GENIChomozygous54084086
7120390296120390297AG43GENIChomozygous54084087
7120390335120390336GA54GENIChomozygous54084088
7120390388120390389GC63GENICpossibly homozygous54084089
7120390852120390853CT64GENIChomozygous54084090
7120390927120390928TC60GENIChomozygous54084091
7120391170120391171AG57GENIChomozygous54084092
7120391780120391781AG51GENIChomozygous54084093
7120392222120392223GA56GENIChomozygous54084094
7120392714120392715CT44GENIChomozygous54084095
7120393749120393750TC46GENIChomozygous54084096
7120394682120394683AACAGCTAGAC17GENIChomozygous54084097
7120394797120394798TC29GENIChomozygous54084098
7120394923120394924TC26GENIChomozygous54084099
7120394944120394945TG18GENIChomozygous54084100
7120395441120395442TC27GENIChomozygous54084101
7120395946120395947TTG26GENICheterozygous54084102
7120395961120395962TTTTG14GENICheterozygous54084103