chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1102794092102794093CCGT8GENICheterozygous60780099
1102794093102794095GT--8GENICheterozygous60780100
1102794267102794268T-8GENICheterozygous60780102
1102797605102797606CCA19GENICheterozygous62515567
1102799297102799299AC--7GENICheterozygous62147363
1102800367102800368AAGC3GENIChomozygous62147365
1102800371102800372CCAGTGGTAGAGCGCTTGCCTAGCAAGCA3GENIChomozygous62147367
1102803100102803102AA--11GENICheterozygous62229322
1102803101102803102A-11GENICheterozygous62147369
1102806453102806454CCTT13GENICheterozygous61299583
1102806454102806455T-13GENICheterozygous62147371
1102809157102809158AAG21GENICheterozygous60780108
1102809157102809158AAGAC21GENICpossibly homozygous60780109
1102813013102813014TTAC10GENICheterozygous62327139
1102813014102813016AC--10GENICpossibly homozygous61299585
1102820713102820715GA--23GENIChomozygous61892447
1102821046102821047CCAAGCA4GENIChomozygous60780111
1102824601102824602AAGGGAGGGAGGGAGGGAGGG1GENIChomozygous62147373
1102830957102830958GGC2GENIChomozygous60780119
1102832818102832821ATA---4GENIChomozygous60780123
1102835290102835292CT--15GENICheterozygous62147377
1102835412102835413TTG47GENIChomozygous60780125
1102835415102835416CT47GENIChomozygous62147379
1102835459102835461TG--34GENIChomozygous60780127
1102837794102837796GG--4GENICheterozygous61486980
1102840078102840079GGTTTTT31GENICheterozygous62147381
1102840085102840086CCT29GENICheterozygous62147383
1102844578102844579CCA2GENICheterozygous62147385
1102847254102847255GGAAAAAAAA6GENIChomozygous62147387
1102848759102848761GG--16GENICheterozygous62147389
1102850224102850225AG17GENICheterozygous62570356