chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1250557300250557301CT6GENIChomozygous61630790
1250557585250557586TTCTC11GENIChomozygous61630791
1250557912250557913TC26GENIChomozygous61630792
1250557966250557967CCCCTAAATACTTGGTCATATAGAACACCAAGCAG26GENIChomozygous62210389
1250558708250558720CACACACACACA------------7GENICheterozygous61630793
1250558710250558720CACACACACA----------7GENICpossibly homozygous61630794
1250559472250559473GA17GENIChomozygous61630795
1250560170250560171CT26GENIChomozygous61630797
1250561839250561840TC18GENIChomozygous61156403
1250561529250561530CA13GENIChomozygous61156400
1250561678250561679CA17GENIChomozygous61156401
1250561827250561828CT13GENIChomozygous61156402
1250561967250561968TC10GENIChomozygous61156404
1250562013250562015AA--9GENICheterozygous62251001
1250562014250562015A-9GENICheterozygous62110558
1250562667250562668TG15GENIChomozygous61156405
1250563105250563106TA17GENIChomozygous61156406
1250563316250563434ACACCCGGGTGTCTTTTTTTTTTTTTTTCTTTTTTCTTTTTTTCGGAGCTGGGGTCCGAACCCAGGGCCTTGCGCTCGCTAGGCAAGCGCTCTACCGCTGAGCTAAATCCCCAACCCC----------------------------------------------------------------------------------------------------------------------28GENIChomozygous62110559
1250563886250563887TC13GENIChomozygous61156407
1250563889250563916TTGTTTTTTTTGTTTTTTTTGTTTTTG---------------------------7GENICpossibly homozygous62210391
1250564487250564488GC28GENIChomozygous61156411
1250564857250564858CT20GENIChomozygous61156412
1250565239250565240GA16GENIChomozygous61156413
1250565288250565289C-9GENICheterozygous61156414
1250565326250565327AG18GENIChomozygous61156415
1250566460250566461GA22GENIChomozygous61156416
1250566673250566674GA14GENIChomozygous61156417