chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5144741980144741981CT51GENICheterozygous114445855
5144741987144741988TA53GENICheterozygous114445857
5144742001144742002TC50GENICheterozygous114445859
5144742009144742010TC46GENICheterozygous114445861
5144746069144746070AG23GENIChomozygous114037693
5144746504144746505TC37GENIChomozygous114037694
5144746634144746635GA19GENICpossibly homozygous114037695
5144746668144746669TC21GENICpossibly homozygous114037696
5144747086144747087GA28GENIChomozygous114037697
5144747796144747797GA38GENICheterozygous114037698
5144748059144748060GC45GENIChomozygous114037699
5144749895144749896AT34GENIChomozygous114037700
5144750770144750771AG49GENIChomozygous114037701
5144751018144751019TC30GENIChomozygous114037702
5144751168144751169AC26GENIChomozygous114037703
5144751607144751608CT43GENICheterozygous114037704
5144751916144751917CG7GENIChomozygous114037705
5144752985144752986CT45GENIChomozygous114037707
5144753208144753209CT25GENIChomozygous114037708
5144755220144755221TC44GENIChomozygous114037709
5144755301144755302CT53GENIChomozygous114037710
5144755308144755309GA51GENIChomozygous114037711
5144756106144756107GA56GENIChomozygous114037712
5144757963144757964TG28GENIChomozygous114037713
5144758049144758050AG33GENIChomozygous114037714
5144758266144758267CT20GENIChomozygous114037715
5144759351144759352TC15GENIChomozygous114037716
5144759359144759360GA23GENICheterozygous114037717
5144759377144759378AG18GENICheterozygous114037718
5144759388144759389CT13GENICpossibly homozygous114037719
5144759427144759428CT23GENIChomozygous114037720
5144759469144759470AC24GENIChomozygous114037721
5144760334144760335AT41GENIChomozygous114037722
5144760661144760662GA31GENIChomozygous114037723