chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1250557300250557301CT8GENIChomozygous61630790
1250557585250557586TTCTC20GENIChomozygous61630791
1250557912250557913TC19GENIChomozygous61630792
1250557966250557967CCCCTAAATACTTGGTCATATAGAACACCAAGCAG27GENIChomozygous62210389
1250558708250558720CACACACACACA------------11GENICheterozygous61630793
1250558710250558720CACACACACA----------11GENICheterozygous61630794
1250559472250559473GA23GENIChomozygous61630795
1250560170250560171CT19GENIChomozygous61630797
1250561529250561530CA15GENIChomozygous61156400
1250561678250561679CA15GENIChomozygous61156401
1250561827250561828CT17GENIChomozygous61156402
1250561839250561840TC14GENIChomozygous61156403
1250561967250561968TC15GENIChomozygous61156404
1250562667250562668TG28GENIChomozygous61156405
1250563105250563106TA22GENIChomozygous61156406
1250563886250563887TC3GENIChomozygous61156407
1250563889250563916TTGTTTTTTTTGTTTTTTTTGTTTTTG---------------------------4GENICheterozygous62210391
1250564487250564488GC28GENIChomozygous61156411
1250564857250564858CT32GENIChomozygous61156412
1250565239250565240GA13GENIChomozygous61156413
1250565287250565289TC--6GENICheterozygous62241401
1250565288250565289C-2GENICheterozygous61156414
1250565326250565327AG12GENIChomozygous61156415
1250566460250566461GA12GENIChomozygous61156416
1250566673250566674GA21GENIChomozygous61156417
1250563316250563434ACACCCGGGTGTCTTTTTTTTTTTTTTTCTTTTTTCTTTTTTTCGGAGCTGGGGTCCGAACCCAGGGCCTTGCGCTCGCTAGGCAAGCGCTCTACCGCTGAGCTAAATCCCCAACCCC----------------------------------------------------------------------------------------------------------------------18GENIChomozygous62110559
1250562014250562015A-5GENIChomozygous62110558