chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
135530691655306917CT23GENIChomozygous49760773
135530693755306938GA22GENIChomozygous49760774
135530703455307035CA20GENIChomozygous49760775
135530714755307148GA24GENIChomozygous49760776
135530722755307230GTG---15GENIChomozygous49760777
135530724155307242GA15GENIChomozygous49760778
135530739955307400AG22GENIChomozygous49760780
135530762855307629CT28GENIChomozygous49760781
135530775155307753AG--22GENIChomozygous49760782
135530788555307886CCTTT20GENICheterozygous49760783
135530788555307886CCTT20GENICheterozygous49760784
135530831655308317GT28GENIChomozygous49760785
135530852455308525TTA29GENICpossibly homozygous49760786
135530853755308538TC31GENIChomozygous49760787
135530883055308834TTTT----6GENIChomozygous50044981
135530929155309292TC21GENIChomozygous49760788
135530951055309511AG28GENIChomozygous49760789
135530974455309745CT17GENIChomozygous49760790
135531069055310691CT27GENIChomozygous49760792
135531143755311438CT18GENIChomozygous49760793
135531219655312197AG24GENIChomozygous49760794