chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4208628227208628228GC42GENIChomozygous57066722
4208628561208628562CT31GENIChomozygous57066723
4208630507208630508CCT1GENIChomozygous57066724
4208630759208630760CCG25GENIChomozygous57066725
4208632116208632117A-12GENIChomozygous57363891
4208632278208632282ATTT----14GENIChomozygous57066727
4208632576208632577CCT13GENICheterozygous57066728
4208632576208632577CCTT13GENICheterozygous58410598
4208632655208632656GA20GENIChomozygous57066729
4208633144208633145AC23GENIChomozygous57066730
4208633280208633281GA23GENIChomozygous57066731
4208633863208633864CT30GENIChomozygous57066732
4208634215208634216CT17GENIChomozygous57066733
4208634482208634483AT14GENIChomozygous57066734
4208635579208635580GA27GENIChomozygous57066735
4208636329208636330TTG18GENIChomozygous57066736
4208636397208636398TC27GENIChomozygous57066737
4208637238208637239TTGCA20GENICpossibly homozygous57066738
4208637477208637478CCTTT11GENICheterozygous58410599
4208637478208637483TTTTT-----11GENICheterozygous57066739
4208637479208637483TTTT----11GENICheterozygous57066740
4208637781208637782CT24GENIChomozygous57066741