chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
45792594557925946CT22GENIChomozygous112659817
45792616357926164GA22GENIChomozygous112659819
45792626157926262GA26GENIChomozygous112659821
45792840757928408CT22GENIChomozygous112659823
45792900657929007TG26GENIChomozygous112659825
45792950657929507CT38GENIChomozygous112659827
45792953557929536AG36GENIChomozygous112659829
45792967157929672GT35GENIChomozygous112659831
45792967257929673GT35GENIChomozygous112659833
45793013157930132CA25GENIChomozygous112659835
45793171157931712GC32GENIChomozygous112659837
45793240757932408CT31GENIChomozygous112659839
45793291657932917TC16GENIChomozygous112659841
45793324157933242GA20GENIChomozygous112659842
45793375357933754CT17GENIChomozygous112659844
45793375657933757AC16GENIChomozygous112659846
45793391557933916CT20GENIChomozygous112659848
45793462857934629CT19GENIChomozygous112659850
45793532157935322TC28GENICpossibly homozygous112659852
45793616657936167TC28GENIChomozygous112659854
45793618557936186TA32GENIChomozygous112659856
45793619857936199CT33GENIChomozygous112659858
45793628457936285TC22GENIChomozygous112659860
45793631857936319AG22GENIChomozygous112659862
45793658657936587TC24GENIChomozygous112659864
45793945857939459TA21GENIChomozygous112659868
45794076357940764TC19GENIChomozygous112659870
45794094557940946GA24GENIChomozygous112659872
45794306757943068AG22GENIChomozygous112659874
45794332557943326AG31GENIChomozygous112659876