chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
182484971124849712TC38GENIChomozygous110309401
182485053424850535GC32GENIChomozygous110679300
182485139924851400CT13GENIChomozygous110309403
182485363524853636GA23GENIChomozygous110309405
182485425624854257TC20GENIChomozygous110309407
182485737724857378CT24GENIChomozygous110309409
182485833924858340TC22GENIChomozygous110309411
182485862124858622TA29GENIChomozygous119485402
182485862924858630AC32GENIChomozygous119485403
182485935724859358GA27GENIChomozygous110309413
182486442724864428GA28GENIChomozygous110647559
182486562324865624TC24GENIChomozygous110309415
182486597524865976TC23GENIChomozygous110309417
182486724324867244GA26GENIChomozygous110812139
182486743624867437AT30GENICpossibly homozygous110309419
182486919224869193AG24GENIChomozygous110309421
182486995424869955AG33GENIChomozygous110309423
182487155724871558TC21GENIChomozygous110309425
182487551824875519TC26GENIChomozygous110309427
182487603124876032AG31GENIChomozygous119485404
182487608324876084CT29GENIChomozygous119485405
182487608924876090GA29GENIChomozygous119485406
182487891524878916TC35GENIChomozygous110309429
182488187524881876AG25GENIChomozygous110309431
182488460524884606AG30GENIChomozygous110309433
182488482524884826AG32GENIChomozygous110309435
182488500324885004CT33GENIChomozygous110309437
182488827524888276GA30GENIChomozygous110309439
182488941224889413CT29GENIChomozygous110309441