chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
172678567726785678CT22GENIChomozygous111010973
172678597826785979AG21GENIChomozygous111010975
172678671826786719AG26GENIChomozygous111010977
172678783026787831AG30GENIChomozygous111398873
172678783126787832TC29GENIChomozygous111398874
172678785626787857AG32GENIChomozygous111237427
172678786626787867AG28GENIChomozygous111398875
172678824926788250TG19GENIChomozygous111010979
172678863426788635CT19GENIChomozygous111010981
172678950826789509CT26GENIChomozygous111010983
172678973626789737CT20GENIChomozygous111398876
172678973826789739AG21GENIChomozygous111237439
172678983426789835AG12GENIChomozygous111010985
172678986826789869GA11GENIChomozygous111010987
172679005926790060AG28GENIChomozygous111010989
172679019226790193TA17GENIChomozygous111010991
172679056826790569AG22GENIChomozygous111398877
172679149026791491AC30GENIChomozygous111010993
172679151326791514GC27GENIChomozygous111010995
172679196526791966CT18GENIChomozygous111010997
172679203626792037AG16GENIChomozygous111010999
172679236426792365GA12GENIChomozygous111011001
172679297226792973CT15GENIChomozygous111011003
172679376726793768CA12GENIChomozygous111011005
172679377526793776GA15GENIChomozygous111011007
172679569926795700AG18GENIChomozygous111398878
172679570226795703AT18GENIChomozygous111398879