chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4189180770189180771AG14GENIChomozygous57995769
4189181774189181775TG27GENIChomozygous59160240
4189182559189182560TTC29GENIChomozygous59160242
4189182580189182581T-16GENIChomozygous58446488
4189182637189182638G-21GENIChomozygous59160244
4189183686189183687CT34GENIChomozygous59160246
4189183721189183722CT31GENIChomozygous59160248
4189184615189184616A-18GENICheterozygous57995778
4189184950189184951AAAAAAAG16GENIChomozygous58484637
4189184453189184454CCA12GENICheterozygous57566375
4189182557189182558GT28GENIChomozygous58484635
4189188352189188353GGTT11GENIChomozygous59160250
4189188406189188407TC4GENIChomozygous57995790
4189188772189188773T-30GENIChomozygous59160252
4189189380189189381T-25GENIChomozygous57995793
4189189589189189590CCTT6GENIChomozygous58484638
4189190858189190859GT29GENIChomozygous59160254
4189191089189191090TC35GENIChomozygous57995802
4189191131189191132AG32GENIChomozygous57995805
4189194190189194191TC23GENIChomozygous57995808
4189194414189194415GA39GENIChomozygous57995811
4189195390189195396TTTTTT------12GENIChomozygous59160256
4189195415189195416CCT13GENIChomozygous57995814
4189197230189197231GA42GENIChomozygous59160258
4189198731189198732TC30GENIChomozygous57995823
4189200013189200014TC26GENIChomozygous57995826
4189200966189200967CT21GENIChomozygous57995829
4189201336189201337AAT26GENIChomozygous59160260
4189201993189201994CG33GENIChomozygous59160262
4189203006189203007GA37GENIChomozygous59160264
4189203587189203588TC23GENIChomozygous57995832
4189203618189203619CCGTGTGTGTGTGTGT4GENIChomozygous59160266
4189203627189203628AG18GENIChomozygous57995835
4189204496189204497AC19GENIChomozygous57995838
4189207592189207593TC36GENIChomozygous57995850
4189208144189208145AC40GENIChomozygous59160268
4189208412189208413TC36GENIChomozygous59160270
4189209357189209358TC33GENIChomozygous57995856
4189209888189209889GT38GENIChomozygous57995862
4189210257189210258AG36GENIChomozygous59160272