chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1227599456227599457TC16GENIChomozygous61602984
1227599867227599868GT12GENIChomozygous61967557
1227599944227599956TTTTCTTTTTCT------------9GENIChomozygous62658200
1227602699227602700AG22GENIChomozygous61105562
1227604153227604154A-17GENIChomozygous61602985
1227604510227604511G-7GENIChomozygous62658201
1227604513227604524TGGAAGGAAGG-----------8GENICpossibly homozygous62658202
1227604700227604701AG12GENIChomozygous61602988
1227605004227605005TC30GENIChomozygous61602989
1227605877227605879TC--2GENIChomozygous62520980
1227605882227605886ATCT----2GENIChomozygous62520982
1227605908227605909CG18GENIChomozygous61602994
1227605914227605915CG23GENIChomozygous61602995
1227605987227605988CG18GENIChomozygous61602996
1227607929227607935CTTCTT------9GENICpossibly homozygous62640532