chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7122204909122204910GA36GENIChomozygous116225921
7122205070122205071TA35GENIChomozygous116225922
7122205357122205358AG43GENIChomozygous116225923
7122205845122205846TC49GENIChomozygous116225924
7122206392122206393GA48GENIChomozygous116225925
7122206413122206414GA43GENIChomozygous116225926
7122208086122208087TC36GENIChomozygous116225927
7122209142122209143TC20GENIChomozygous116225928
7122209147122209148TC30GENIChomozygous116225929
7122209207122209208CT27GENIChomozygous122851673
7122209314122209314T16GENIChomozygous128513214
7122207896122207897T33GENIChomozygous128513210
7122209198122209207CCCCCCGCA26GENIChomozygous128513211
7122209211122209211AAAGATTTAT26GENIChomozygous128513212
7122209221122209221T24GENIChomozygous128513213
7122207899122207900TG33GENIChomozygous115860320
7122207900122207901CG33GENIChomozygous115860322
7122208836122208839TCT34GENIChomozygous132657536
7122209347122209348GC10GENIChomozygous115860324
7122209349122209350AC9GENIChomozygous115860326
7122209366122209367AC8GENIChomozygous115860328
7122209370122209371GC8GENIChomozygous115860330
7122209496122209497GC25GENIChomozygous115860332
7122209514122209515GC27GENIChomozygous115860334
7122209526122209527GC28GENIChomozygous115860336
7122210446122210447A19GENIChomozygous131433911
7122210617122210617GAGGCA14GENIChomozygous132657537
7122210878122210878A33GENIChomozygous132657538
7122212538122212539GA45GENIChomozygous116225930
7122216161122216162TA47GENIChomozygous116225931
7122223476122223477C39GENICpossibly homozygous131433913
7122223933122223934TC50GENIChomozygous116225932
7122224644122224645CT34GENIChomozygous116225933
7122225043122225044GA39GENIChomozygous116225934
7122225715122225716TC45GENIChomozygous116225935
7122227870122227871TC43GENIChomozygous116225936
7122229390122229391AG53GENIChomozygous116225937
7122229412122229413TC50GENIChomozygous116225938
7122229684122229685AG55GENICpossibly homozygous116225939
7122231302122231303TC48GENIChomozygous116225940