chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104652416046524161AACAG14GENIChomozygous51444852
104652449946524500TC13GENIChomozygous51444853
104652503046525031GGA13GENIChomozygous51444855
104652553046525531AG10GENIChomozygous51444856
104652624846526249GC11GENIChomozygous51444857
104652665546526656AAT10GENIChomozygous51444858
104652704546527046AG15GENIChomozygous51444859
104652749846527499CT13GENIChomozygous51444860
104652752046527522CA--9GENIChomozygous52497287
104652842146528422GA13GENIChomozygous51444861
104652843446528435CG13GENIChomozygous52497289
104652859546528596CT9GENIChomozygous51444862
104652878746528788GC16GENIChomozygous51444863
104652895446528955CT18GENIChomozygous52497291
104653182146531822AT5GENIChomozygous51444864
104653294446532945GA8GENIChomozygous52497293
104653357046533571GA14GENIChomozygous51444867
104653436646534367GGT6GENIChomozygous51444868
104653445746534458CT8GENIChomozygous51444869
104653518346535184CCA4GENIChomozygous52497295
104653536846535369TG9GENIChomozygous51444870
104653614346536144C-13GENIChomozygous51444871
104653740846537409AC9GENIChomozygous51444872
104653766846537669GA6GENIChomozygous52053506
104653778546537786CCT6GENIChomozygous51444873
104653782846537829CT17GENIChomozygous52053508
104653796446537965GA12GENIChomozygous51444874
104653886746538868GA5GENIChomozygous51444876