chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4145028086145028087GT33GENIChomozygous112870577
4145035856145035857GA43GENIChomozygous112870578
4145036128145036129AT27GENIChomozygous112870579
4145036206145036207CA39GENIChomozygous112870580
4145036438145036439TC38GENIChomozygous112870581
4145037242145037243AG50GENIChomozygous112870582
4145048390145048391GA35GENIChomozygous112870583
4145066093145066094TA40GENICheterozygous112870585
4145067100145067101GA50GENIChomozygous112870586
4145069675145069676AG41GENIChomozygous112870587
4145071023145071024CT29GENIChomozygous112870588
4145071061145071062TC35GENICpossibly homozygous112870589
4145072901145072902GA36GENIChomozygous112870590
4145077693145077694GA59GENIChomozygous112870591
4145078162145078163AG52GENIChomozygous112870592
4145078803145078804TC41GENIChomozygous112870593
4145080276145080277CA41GENICheterozygous113562725
4145080487145080488AG58GENIChomozygous112870594
4145081503145081504AG24GENIChomozygous112870595
4145083087145083088TG33GENICheterozygous113178966
4145083460145083461CT49GENIChomozygous112870596
4145084002145084003AG52GENIChomozygous112870597
4145084914145084915TC60GENIChomozygous112870598
4145085708145085709CT65GENIChomozygous112870599
4145089767145089768CT48GENIChomozygous112870600
4145092714145092715GA53GENIChomozygous112870601
4145095105145095106CG44GENICheterozygous112870602
4145095113145095114GT42GENICheterozygous112870603
4145095121145095122GA51GENICheterozygous112870604
4145095124145095125AG53GENICheterozygous112870605
4145095154145095155GA50GENICheterozygous112870606
4145095188145095189GA58GENICheterozygous112870607
4145095191145095192AG61GENICheterozygous112870608
4145095221145095222TC68GENICheterozygous112870610
4145095112145095113GA42GENICheterozygous113058853
4145095209145095210GC66GENICheterozygous112870609