chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7122206547122206548GT13GENIChomozygous118418333
7122207651122207652TC17GENIChomozygous118418334
7122209421122209422CG13GENIChomozygous126539208
7122212538122212539GA5GENIChomozygous116225930
7122213905122213906CT20GENIChomozygous118418337
7122214100122214101GA13GENIChomozygous118418338
7122216161122216162TA19GENIChomozygous116225931
7122220891122220892GC15GENICheterozygous118418339
7122221714122221715AG16GENIChomozygous118418340
7122222709122222710GA5GENIChomozygous118418342
7122223479122223480CA6GENICheterozygous126648003
7122209752122209753AG23GENIChomozygous126648000
7122211139122211140AG18GENIChomozygous126648001
7122217805122217806TC3GENICheterozygous126648002
7122223634122223635CT15GENIChomozygous118418343
7122223933122223934TC20GENICpossibly homozygous116225932
7122225715122225716TC10GENIChomozygous116225935
7122227870122227871TC18GENIChomozygous116225936
7122227933122227934AG22GENIChomozygous118418344
7122229412122229413TC4GENIChomozygous116225938
7122229684122229685AG8GENIChomozygous116225939
7122231302122231303TC10GENIChomozygous116225940