chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3112229354112229355TC14GENIChomozygous111675464
3112230595112230596CA15GENIChomozygous111675467
3112235873112235873T7GENIChomozygous127918838
3112231032112231033TC10GENIChomozygous112292698
3112235837112235837T3GENIChomozygous127918834
3112235857112235858C6GENIChomozygous127918835
3112235864112235865T7GENIChomozygous127918836
3112235868112235868C7GENIChomozygous127918837
3112235818112235819TC5GENIChomozygous130290274
3112235820112235820T5GENIChomozygous130282597
3112235835112235836TC3GENIChomozygous127988682
3112235837112235838AC3GENIChomozygous127988683
3112235839112235840GC4GENIChomozygous127988684
3112235842112235843TC4GENIChomozygous127988685
3112235914112235914T11GENIChomozygous127918842
3112235895112235895T10GENIChomozygous127918839
3112235901112235903GA10GENIChomozygous127918840
3112235908112235908GC10GENIChomozygous127918841
3112235923112235924C12GENIChomozygous127918843
3112235942112235943CT15GENIChomozygous111675479
3112235946112235946C15GENIChomozygous127918844
3112235949112235949T15GENIChomozygous127918845
3112235963112235965AA16GENIChomozygous127918846
3112235971112235971G16GENIChomozygous127918847
3112235975112235977CC16GENIChomozygous127918848
3112236011112236012G17GENIChomozygous127918849
3112236033112236034TG16GENIChomozygous121853560
3112236035112236036G16GENIChomozygous127918850
3112236046112236047G14GENIChomozygous127918851
3112236050112236052CC13GENIChomozygous127918852
3112236056112236057T13GENIChomozygous127918853
3112236063112236063T15GENIChomozygous127918854
3112236065112236065G15GENIChomozygous127918855
3112236073112236076ACT17GENIChomozygous127918856
3112236087112236089TG18GENIChomozygous127918857
3112236096112236097T18GENIChomozygous127918858
3112236141112236142G20GENIChomozygous127918859
3112236152112236152ATGCCTTTTCCCAC19GENIChomozygous127918860
3112240428112240428A3GENIChomozygous127918862
3112250114112250114ACTGGCTTGTTTTTGGCTTGCTCAGCCTG4GENIChomozygous130282598