chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71225864212258643GT31GENICpossibly homozygous115569715
71225892712258928GC12GENIChomozygous116316529
71225895412258955GC13GENICheterozygous116316531
71225906512259066AG23GENIChomozygous116316533
71226051012260511GT31GENICpossibly homozygous116274516
71226142612261427AG36GENIChomozygous115569720
71226210412262105AG34GENIChomozygous116316535
71226295812262959GA25GENIChomozygous116274520
71226331212263313AG29GENIChomozygous116274522
71226397512263976GA37GENIChomozygous116316537
71226486112264862AG35GENIChomozygous116274524
71226500112265002TC45GENIChomozygous116274526
71226501812265019AG39GENIChomozygous115569725
71226708012267081AG37GENIChomozygous116274530
71226756612267567GT48GENIChomozygous115569726
71226826312268264GA30GENIChomozygous116316539
71226884912268850CT44GENICheterozygous116316541
71226895912268960CT48GENIChomozygous116316543
71227127512271276TC51GENIChomozygous115569728
71227246512272466CT28GENIChomozygous116316545
71227293312272934AT41GENIChomozygous116316547
71227304912273050GT25GENIChomozygous116316549
71227322912273230TC21GENIChomozygous115569729
71227371512273716GA40GENIChomozygous116316551
71227381012273811CG44GENIChomozygous115569730
71227393612273937GA26GENIChomozygous116316553
71227455112274552TG40GENIChomozygous115569731
71227459912274600CT31GENIChomozygous116316555
71227543212275433TC26GENIChomozygous115569734
71227561112275612TC40GENIChomozygous115569735
71227569712275698TC44GENIChomozygous115569736
71227570012275701TG44GENIChomozygous115569737
71227633412276335TC23GENIChomozygous115569739
71227694212276943CT35GENIChomozygous116316557
71227802112278022CT29GENICpossibly homozygous116316559
71227878012278781TC31GENIChomozygous115569742
71227898812278989CT51GENIChomozygous116316561
71227925212279253AG22GENIChomozygous115569744
71227965612279657GA29GENIChomozygous116316563
71227978612279787GT34GENIChomozygous116316565