chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7123599813123599814GGT47INTERGENICheterozygous54090427
7123600671123600672TG29INTERGENIChomozygous54236856
7123600985123600986GA22INTERGENIChomozygous54090436
7123603119123603120CA26GENIChomozygous54090454
7123603124123603125CA27GENIChomozygous54090456
7123604465123604466GGTC13GENICheterozygous54090467
7123604497123604498GC20GENIChomozygous54090468
7123604570123604571AATG18GENIChomozygous54236862
7123605258123605259TG16GENIChomozygous54090470
7123606265123606266CT18INTERGENIChomozygous54236864
7123606581123606582AG35INTERGENIChomozygous54090471
7123607896123607897GA34INTERGENIChomozygous54236866
7123604465123604466GGTCTC13GENICheterozygous55361956