chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3165520220165520220A33GENIChomozygous127953065
3165520323165520324GA26GENIChomozygous111809046
3165520728165520729AG54GENIChomozygous111809048
3165521148165521148A29GENICpossibly homozygous127953066
3165521232165521233AG30GENIChomozygous111809050
3165523438165523439AG37GENIChomozygous111809052
3165524626165524627AG43GENIChomozygous111809054
3165524659165524660AG42GENIChomozygous111809056
3165524983165524984TC46GENIChomozygous111809058
3165525934165525935CT49GENIChomozygous111809060
3165526208165526211AAC33GENIChomozygous127953067
3165527136165527137G11GENIChomozygous127953068
3165527174165527175C10GENIChomozygous127953069
3165527208165527209A15GENIChomozygous127953070
3165527219165527220G16GENIChomozygous127953071
3165527226165527227A16GENIChomozygous127953072
3165527318165527320GA15GENIChomozygous127953073
3165527357165527357A9GENIChomozygous127953074
3165527380165527381AC9GENIChomozygous111809062
3165527384165527385C10GENIChomozygous127953075
3165527388165527390CC11GENIChomozygous127953076
3165527549165527550A21GENIChomozygous127953077
3165528715165528715A30GENIChomozygous127953078
3165528955165528956TC29GENIChomozygous111809064
3165529170165529186ATATACATATATATGC11GENICheterozygous127953079
3165531506165531506T17GENIChomozygous127953080
3165532589165532590GA31GENIChomozygous111809066
3165533430165533430CT13GENIChomozygous127953081
3165534595165534596GA40GENIChomozygous111809068
3165534988165534989TG40GENIChomozygous111809070
3165535343165535344TC58GENIChomozygous111809072
3165535779165535780TA45GENIChomozygous111809074
3165535829165535829AA43GENIChomozygous127953082
3165536921165536921AAT26GENIChomozygous127953083
3165536923165536924CG27GENIChomozygous119652754
3165536919165536920CG26GENIChomozygous119652753
3165536925165536928CCC26GENIChomozygous127953084
3165536928165536929CG26GENIChomozygous119652755