chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3165520220165520220A10GENIChomozygous127953065
3165520323165520324GA6GENIChomozygous111809046
3165520728165520729AG16GENIChomozygous111809048
3165521148165521148A16GENICpossibly homozygous127953066
3165521232165521233AG22GENIChomozygous111809050
3165523438165523439AG23GENIChomozygous111809052
3165524626165524627AG20GENIChomozygous111809054
3165524659165524660AG19GENIChomozygous111809056
3165524983165524984TC18GENIChomozygous111809058
3165525934165525935CT17GENIChomozygous111809060
3165526208165526211AAC16GENIChomozygous127953067
3165527136165527137G7GENIChomozygous127953068
3165527174165527175C6GENIChomozygous127953069
3165527208165527209A5GENIChomozygous127953070
3165527219165527220G5GENIChomozygous127953071
3165527226165527227A5GENIChomozygous127953072
3165527318165527320GA6GENIChomozygous127953073
3165527357165527357A7GENIChomozygous127953074
3165527380165527381AC8GENIChomozygous111809062
3165527384165527385C8GENIChomozygous127953075
3165527388165527390CC7GENIChomozygous127953076
3165527549165527550A11GENIChomozygous127953077
3165528715165528715A9GENICpossibly homozygous127953078
3165528955165528956TC10GENIChomozygous111809064
3165529170165529186ATATACATATATATGC8GENIChomozygous127953079
3165531506165531506T7GENIChomozygous127953080
3165532589165532590GA14GENIChomozygous111809066
3165533430165533430CT3GENIChomozygous127953081
3165534595165534596GA12GENIChomozygous111809068
3165534988165534989TG14GENIChomozygous111809070
3165535343165535344TC20GENIChomozygous111809072
3165535779165535780TA16GENIChomozygous111809074
3165535829165535829AA15GENIChomozygous127953082
3165536921165536921AAT9GENIChomozygous127953083
3165536925165536928CCC8GENIChomozygous127953084
3165529349165529349GG1GENIChomozygous131332098
3165529350165529350AAAAAGGGGGGTTGGAGAGATGGCTCAGTGGTTAGG1GENIChomozygous131332099
3165536919165536920CG9GENIChomozygous119652753
3165536923165536924CG8GENIChomozygous119652754
3165536928165536929CG8GENIChomozygous119652755