chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1225334305225334306AT13GENIChomozygous61600669
1225334426225334427CT15GENIChomozygous61807362
1225334502225334503AG5GENIChomozygous61807363
1225334850225334851AG25GENIChomozygous61600671
1225335555225335556AC26GENIChomozygous61600673
1225336120225336121TG32GENIChomozygous61600675
1225336157225336161GGGG----15GENIChomozygous61600676
1225336477225336478GA12GENIChomozygous61807364
1225336714225336715TC26GENIChomozygous61101600
1225336863225336864GA20GENIChomozygous61600680
1225337408225337409CT34GENIChomozygous61807365
1225338049225338050GA47GENIChomozygous61600682
1225338356225338357GGCTATTCACTATTTGCTATTCA32GENICpossibly homozygous62520673
1225338580225338581AG28GENIChomozygous61600690
1225338636225338638TT--24GENIChomozygous61600692
1225338637225338638TC22GENIChomozygous62546807
1225338846225338847AC30GENIChomozygous61807366
1225338956225338957CT30GENIChomozygous61600695
1225339093225339094AG27GENIChomozygous61600697
1225339553225339554CCAGAG35GENIChomozygous61101610
1225339685225339686AG40GENIChomozygous61101611
1225339823225339848TTTCTTTTCTTTTCTTTTCTTTTCT-------------------------14GENIChomozygous62540079
1225340000225340001AG24GENIChomozygous61600705
1225340416225340417TG17GENIChomozygous61600706
1225340595225340597AA--19GENIChomozygous61807367
1225341238225341239TC35GENIChomozygous61600712
1225341295225341296AT35GENIChomozygous62540080
1225343131225343132AG19GENIChomozygous61600718
1225343981225343982CA31GENIChomozygous61101619