chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4145025139145025140CG40GENICheterozygous112870576
4145028086145028087GT35GENIChomozygous112870577
4145035856145035857GA36GENIChomozygous112870578
4145036206145036207CA33GENIChomozygous112870580
4145036438145036439TC34GENIChomozygous112870581
4145037242145037243AG15GENIChomozygous112870582
4145048390145048391GA25GENIChomozygous112870583
4145066093145066094TA42GENICheterozygous112870585
4145067100145067101GA42GENIChomozygous112870586
4145069675145069676AG25GENIChomozygous112870587
4145071023145071024CT23GENIChomozygous112870588
4145071061145071062TC12GENIChomozygous112870589
4145072901145072902GA20GENIChomozygous112870590
4145077693145077694GA30GENIChomozygous112870591
4145078162145078163AG22GENIChomozygous112870592
4145078803145078804TC34GENIChomozygous112870593
4145080487145080488AG20GENIChomozygous112870594
4145081503145081504AG35GENICpossibly homozygous112870595
4145083460145083461CT24GENIChomozygous112870596
4145084002145084003AG29GENIChomozygous112870597
4145084914145084915TC13GENIChomozygous112870598
4145085708145085709CT12GENIChomozygous112870599
4145089767145089768CT26GENIChomozygous112870600
4145092714145092715GA30GENIChomozygous112870601
4145095105145095106CG34GENICheterozygous112870602
4145095113145095114GT37GENICheterozygous112870603
4145095121145095122GA38GENICheterozygous112870604
4145095124145095125AG38GENICheterozygous112870605
4145095154145095155GA40GENICheterozygous112870606
4145095188145095189GA39GENICheterozygous112870607
4145095191145095192AG37GENICheterozygous112870608
4145095209145095210GC33GENICheterozygous112870609
4145095221145095222TC30GENICheterozygous112870610
4145095112145095113GA35GENICheterozygous113058853