chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2203532416203532417TG36GENIChomozygous75087011
2203532893203532894AC22GENICpossibly homozygous75087013
2203532965203532966AG34GENICpossibly homozygous75087015
2203533753203533754AG29GENIChomozygous75087017
2203534130203534131GA50GENIChomozygous75087019
2203534305203534306AG25GENIChomozygous75087021
2203534319203534320GT23GENIChomozygous75087023
2203534919203534920AC28GENIChomozygous75087025
2203535000203535001GA51GENICpossibly homozygous75087027
2203535332203535333TC36GENIChomozygous75087029
2203535816203535817CT59GENICheterozygous74283784
2203535831203535832CA61GENICheterozygous74283787
2203535953203535954CG45GENICpossibly homozygous75087031
2203536920203536921AC32GENIChomozygous75087033