chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7122206546122206547G16GENIChomozygous131433910
7122206547122206548GT16GENIChomozygous118418333
7122207651122207652TC18GENIChomozygous118418334
7122209207122209208CT9GENIChomozygous122851673
7122209314122209314T12GENIChomozygous128513214
7122207896122207897T19GENIChomozygous128513210
7122209198122209207CCCCCCGCA9GENIChomozygous128513211
7122209211122209211AAAGATTTAT9GENIChomozygous128513212
7122209221122209221T8GENIChomozygous128513213
7122207899122207900TG18GENIChomozygous115860320
7122207900122207901CG18GENIChomozygous115860322
7122209347122209348GC12GENIChomozygous115860324
7122209349122209350AC12GENIChomozygous115860326
7122209366122209367AC12GENIChomozygous115860328
7122209370122209371GC10GENIChomozygous115860330
7122210446122210447A16GENIChomozygous131433911
7122214100122214101GA22GENIChomozygous118418338
7122209496122209497GC8GENIChomozygous115860332
7122209514122209515GC7GENIChomozygous115860334
7122209526122209527GC6GENIChomozygous115860336
7122212538122212539GA30GENIChomozygous116225930
7122213905122213906CT22GENIChomozygous118418337
7122209754122209755TC5GENIChomozygous131440517
7122216161122216162TA24GENIChomozygous116225931
7122217233122217233T2GENIChomozygous131433912
7122220891122220892GC23GENIChomozygous118418339
7122221714122221715AG21GENIChomozygous118418340
7122222709122222710GA18GENIChomozygous118418342
7122223476122223477C15GENIChomozygous131433913
7122223634122223635CT26GENIChomozygous118418343
7122223933122223934TC17GENIChomozygous116225932
7122225715122225716TC23GENIChomozygous116225935
7122227870122227871TC22GENIChomozygous116225936
7122227933122227934AG23GENIChomozygous118418344
7122229390122229391AG27GENIChomozygous116225937
7122229412122229413TC26GENIChomozygous116225938
7122229684122229685AG21GENIChomozygous116225939
7122231302122231303TC27GENIChomozygous116225940