chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104652416046524161AACAG18GENIChomozygous51444852
104652449946524500TC25GENIChomozygous51444853
104652464046524641AC17GENIChomozygous51444854
104652503046525031GGA25GENIChomozygous51444855
104652553046525531AG30GENIChomozygous51444856
104652624846526249GC17GENIChomozygous51444857
104652665546526656AAT21GENIChomozygous51444858
104652704546527046AG35GENIChomozygous51444859
104652749846527499CT20GENIChomozygous51444860
104652842146528422GA22GENIChomozygous51444861
104652859546528596CT20GENIChomozygous51444862
104652878746528788GC28GENIChomozygous51444863
104653182146531822AT10GENIChomozygous51444864
104653232346532324A-9GENICheterozygous51444865
104653277646532777CT6GENIChomozygous51444866
104653357046533571GA24GENIChomozygous51444867
104653436646534367GGT10GENIChomozygous51444868
104653445746534458CT16GENIChomozygous51444869
104653536846535369TG27GENIChomozygous51444870
104653614346536144C-18GENIChomozygous51444871
104653740846537409AC20GENIChomozygous51444872
104653778546537786CCT8GENICpossibly homozygous51444873
104653778546537786CCTTT8GENICheterozygous51636980
104653796446537965GA24GENIChomozygous51444874
104653861646538617GA20GENIChomozygous51444875
104653886746538868GA8GENIChomozygous51444876