chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7143897818143897819AG3GENIChomozygous126541605
7143898110143898111CT2GENIChomozygous126541606
7143898896143898897TA3GENIChomozygous126541608
7143899130143899131TG2GENIChomozygous126541609
7143908992143908993CT4GENIChomozygous126541628
7143909021143909022GA5GENIChomozygous126541629
7143909402143909403TC10GENIChomozygous115944782
7143909478143909479TC13GENIChomozygous115944783
7143911536143911537CA19GENIChomozygous115944784
7143913006143913007AG17GENIChomozygous115944785
7143913815143913816AG19GENIChomozygous115944786
7143916696143916696AGTGCCTCCAT18GENIChomozygous128531518
7143910312143910313C5GENIChomozygous128531515
7143911772143911772AGAG21GENIChomozygous128531516
7143914697143914698T5GENIChomozygous128531517
7143919631143919631ATTA10GENIChomozygous128531519
7143921070143921070TT8GENICpossibly homozygous128531520