chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1102793018102793019CCT7GENICheterozygous62229320
1102793414102793418AAAG----5GENICheterozygous62341900
1102794093102794095GT--10GENICheterozygous60780100
1102794267102794268T-10GENICheterozygous60780102
1102799297102799299AC--9GENICheterozygous62147363
1102800367102800368AAGC2GENIChomozygous62147365
1102800371102800372CCAGTGGTAGAGCGCTTGCCTAGCAAGCA2GENIChomozygous62147367
1102803101102803102A-12GENICpossibly homozygous62147369
1102809157102809158AAG18GENICheterozygous60780108
1102809157102809158AAGAC18GENICheterozygous60780109
1102813013102813014TTAC15GENICheterozygous62327139
1102813014102813016AC--15GENICpossibly homozygous61299585
1102820713102820715GA--9GENIChomozygous61892447
1102821046102821047CCAAGCA2GENIChomozygous60780111
1102830957102830958GGC1GENIChomozygous60780119
1102831919102831920T-10GENICheterozygous61486959
1102832017102832061CAGCCCTCTTATGTGTGTTTTGATAATTGTGTTTCCCAAGGCTT--------------------------------------------16GENICheterozygous62147375
1102832818102832821ATA---3GENIChomozygous60780123
1102835412102835413TTG42GENIChomozygous60780125
1102835415102835416CT41GENIChomozygous62147379
1102835459102835461TG--35GENIChomozygous60780127
1102840078102840079GGTTTTT23GENICheterozygous62147381
1102840085102840086CCT22GENICheterozygous62147383
1102844578102844579CCA2GENICheterozygous62147385
1102845218102845220AC--20GENICheterozygous62229325
1102847254102847255GGAAAAAAAA6GENIChomozygous62147387
1102848759102848761GG--14GENICheterozygous62147389