chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4189180770189180771AG2GENIChomozygous57995769
4189181774189181775TG20GENIChomozygous59160240
4189182559189182560TTC4GENIChomozygous59160242
4189182580189182581T-6GENIChomozygous58446488
4189182637189182638G-1GENIChomozygous59160244
4189183686189183687CT21GENIChomozygous59160246
4189183721189183722CT25GENIChomozygous59160248
4189184615189184616A-2GENIChomozygous57995778
4189184950189184951AAAAAAAG3GENIChomozygous58484637
4189182557189182558GT3GENIChomozygous58484635
4189188352189188353GGTT2GENIChomozygous59160250
4189188772189188773T-26GENIChomozygous59160252
4189189380189189381T-3GENIChomozygous57995793
4189190858189190859GT20GENIChomozygous59160254
4189191089189191090TC7GENIChomozygous57995802
4189191131189191132AG17GENIChomozygous57995805
4189194190189194191TC24GENIChomozygous57995808
4189194414189194415GA11GENIChomozygous57995811
4189197230189197231GA23GENIChomozygous59160258
4189198731189198732TC20GENICpossibly homozygous57995823
4189200013189200014TC12GENIChomozygous57995826
4189200966189200967CT15GENIChomozygous57995829
4189201336189201337AAT2GENICheterozygous59160260
4189201993189201994CG28GENICpossibly homozygous59160262
4189203006189203007GA25GENICpossibly homozygous59160264
4189203587189203588TC12GENIChomozygous57995832
4189203627189203628AG8GENIChomozygous57995835
4189204496189204497AC28GENICpossibly homozygous57995838
4189207592189207593TC15GENIChomozygous57995850
4189208144189208145AC18GENICpossibly homozygous59160268
4189208412189208413TC21GENICpossibly homozygous59160270
4189209357189209358TC8GENICpossibly homozygous57995856
4189209888189209889GT21GENIChomozygous57995862
4189210257189210258AG16GENICpossibly homozygous59160272