chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1199088332199088333GT16GENIChomozygous615896919
1199090507199090510TTT---16GENICheterozygous736040863
1199090508199090510TT--16GENICheterozygous736040864
1199090509199090510T-16GENICheterozygous736040865
1199093432199093433TC25GENIChomozygous615896920
1199093873199093874GA25GENIChomozygous613628601
1199093919199093920CCTTTTT12GENICheterozygous736040866
1199093919199093920CCTTTTTT12GENICheterozygous736040867
1199094029199094030A-24GENIChomozygous736040868
1199094082199094085CTG---15GENIChomozygous736040869
1199094538199094547TTTTTTTTT---------13GENICheterozygous736040870
1199094539199094547TTTTTTTT--------13GENICheterozygous736040871
1199094981199094982AG38GENIChomozygous613628602
1199095171199095172GT36GENIChomozygous615896921
1199095810199095811AG30GENIChomozygous613628603
1199095971199095972AAT5GENIChomozygous736040872
1199095979199095980CT3GENICheterozygous615896922
1199096830199096831GGC27GENIChomozygous736040873
1199097532199097533GC26GENIChomozygous615896923
1199098345199098346T-27GENICpossibly homozygous736040874
1199099660199099661T-22GENIChomozygous736040875
1199099914199099915TTG21GENIChomozygous736040876
1199101093199101106GCTCCTTGTCCCA-------------27GENIChomozygous736040877