chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7141480601141480602TA24GENICpossibly homozygous54159116
7141480655141480656CT19GENICheterozygous55960901
7141480752141480753C-22GENIChomozygous54159117
7141480988141480989GA12GENIChomozygous55960902
7141481025141481026AAT14GENICpossibly homozygous55960903
7141485203141485204TC26GENIChomozygous54159123
7141487235141487236TTG8GENIChomozygous54159125
7141487569141487570AC19GENICpossibly homozygous54159127
7141487924141487925CT5GENIChomozygous54159128
7141490175141490176GC15GENICpossibly homozygous54159130
7141491369141491370T-6GENIChomozygous54159132
7141491432141491433AG16GENIChomozygous54159133
7141491721141491722GGC3GENIChomozygous55960904
7141491737141491738C-4GENIChomozygous54159134
7141491916141491917GA12GENICpossibly homozygous54159136
7141492007141492008TG10GENIChomozygous55960905
7141492597141492598AG27GENICpossibly homozygous54159137
7141493142141493143A-1GENIChomozygous55470279
7141493733141493734GA18GENIChomozygous54159142
7141494160141494161TC6GENIChomozygous54159143
7141494234141494238AAAG----1GENIChomozygous55960906
7141494241141494242CCA2GENICheterozygous55017120
7141494242141494244AA--2GENICheterozygous54159144
7141496672141496673T-3GENICheterozygous54159147
7141496762141496763TC14GENICpossibly homozygous54159149