chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7120387249120387250GA32GENIChomozygous54084081
7120387941120387942TC35GENIChomozygous54084082
7120389509120389510CT32GENIChomozygous54084084
7120389607120389608AG32GENICpossibly homozygous54084085
7120389713120389714AG18GENIChomozygous54084086
7120390296120390297AG37GENIChomozygous54084087
7120390388120390389GC41GENIChomozygous54084089
7120390927120390928TC26GENIChomozygous54084091
7120391170120391171AG29GENIChomozygous54084092
7120391780120391781AG30GENIChomozygous54084093
7120392222120392223GA40GENIChomozygous54084094
7120392936120392937GA43GENIChomozygous54234171
7120393749120393750TC31GENIChomozygous54084096
7120394682120394683AACAGCTAGAC20GENIChomozygous54084097
7120394797120394798TC21GENIChomozygous54084098
7120394923120394924TC17GENIChomozygous54084099
7120394944120394945TG11GENIChomozygous54084100
7120395441120395442TC20GENIChomozygous54084101
7120395940120395952TTTTTTTTTTTT------------15GENIChomozygous54234173
7120396585120396586TTC12GENICpossibly homozygous54234175