chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4208628227208628228GC57GENIChomozygous57066722
4208628561208628562CT70GENIChomozygous57066723
4208630507208630508CCT6GENICheterozygous57066724
4208630759208630760CCG55GENIChomozygous57066725
4208631169208631170GA32GENICheterozygous57066726
4208632278208632282ATTT----57GENIChomozygous57066727
4208632576208632577CCT41GENIChomozygous57066728
4208632655208632656GA47GENICpossibly homozygous57066729
4208633144208633145AC56GENIChomozygous57066730
4208633280208633281GA52GENIChomozygous57066731
4208633863208633864CT63GENIChomozygous57066732
4208634215208634216CT52GENIChomozygous57066733
4208634482208634483AT52GENIChomozygous57066734
4208635579208635580GA56GENIChomozygous57066735
4208636329208636330TTG52GENIChomozygous57066736
4208636397208636398TC59GENICpossibly homozygous57066737
4208637238208637239TTGCA36GENICpossibly homozygous57066738
4208637478208637483TTTTT-----2GENICheterozygous57066739
4208637479208637483TTTT----2GENICheterozygous57066740
4208637781208637782CT41GENIChomozygous57066741
4208632116208632117A-1GENIChomozygous57363891