chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1185109520185109521GA15GENIChomozygous62094604
1185110192185110193CG11GENIChomozygous61000801
1185112775185112776AG8GENIChomozygous61000809
1185113329185113333ATCT----9GENIChomozygous61000810
1185117305185117306AG7GENIChomozygous62094605
1185121051185121052A-3GENIChomozygous62094606
1185121835185121836GGTAAA4GENIChomozygous61000818
1185122780185122781GA20GENIChomozygous61000819
1185123499185123500GA5GENICheterozygous61000820
1185123769185123770AG11GENIChomozygous62094607
1185125077185125078CT19GENICpossibly homozygous62094608
1185133442185133443TTA2GENICheterozygous62094609
1185133589185133590GA10GENIChomozygous62094610
1185142986185142987A-2GENIChomozygous62094611
1185145963185145964A-5GENIChomozygous61000845
1185148734185148752TTGACTAGCTGGCGTTCC------------------2GENIChomozygous62094612
1185150556185150557AC12GENIChomozygous61000860
1185151389185151390CT12GENICpossibly homozygous61000861
1185152126185152127TTAAA4GENICheterozygous61313406
1185154377185154378GGA2GENICheterozygous61000869
1185154932185154933AAC5GENIChomozygous61000871
1185155809185155810GA23GENIChomozygous61000873
1185157617185157618TTGCCC4GENIChomozygous62094613
1185159285185159286CT15GENIChomozygous62094614
1185159380185159381TC18GENICpossibly homozygous61000875
1185159758185159759TA18GENIChomozygous61000877
1185164293185164294AC4GENIChomozygous61000882