chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4123639391123639392GA29GENIChomozygous113156021
4123639741123639742CT37GENIChomozygous113156022
4123639910123639911GA37GENIChomozygous119358607
4123639911123639912GA38GENIChomozygous119358609
4123640627123640628GC42GENIChomozygous113156023
4123641673123641674CG37GENIChomozygous113156024
4123643320123643321AG43GENIChomozygous113156025
4123646459123646460AG36GENIChomozygous113156026
4123648771123648772TC26GENIChomozygous113156027
4123652606123652607AG39GENIChomozygous113156028
4123660636123660637AG36GENIChomozygous113156029
4123661145123661146CA36GENIChomozygous113156030
4123664940123664941GT44GENIChomozygous112825547
4123666659123666660GA18GENIChomozygous119346894
4123666660123666661AC18GENIChomozygous119346896
4123667174123667175TA27GENIChomozygous119280282
4123667175123667176AT27GENIChomozygous119280284
4123667500123667501AG19GENIChomozygous112825565
4123667696123667697GC30GENIChomozygous112825567
4123667799123667800GA30GENIChomozygous113156032
4123675270123675271GA41GENIChomozygous113156033
4123685198123685199TC38GENIChomozygous113156034
4123698351123698352TC21GENIChomozygous113156035
4123702489123702490GT41GENIChomozygous113156036
4123702553123702554GA41GENIChomozygous113156037
4123706579123706580TC34GENIChomozygous113156038
4123709103123709104TC24GENIChomozygous113156040
4123710195123710196AT46GENIChomozygous113156041
4123713099123713100CT39GENIChomozygous113156042