chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1128950285128950286AG8GENICpossibly homozygous60850269
1128954639128954640G-11GENICheterozygous60850270
1128961609128961610AAGT5GENICheterozygous62296866
1129036108129036109GGT20GENIChomozygous60850372
1129043673129043674C-3GENIChomozygous60850394
1129043680129043681CG4GENIChomozygous60850395
1129043758129043759CT2GENICheterozygous60850397
1129047226129047227CA19GENICheterozygous60850411
1129047255129047256CA20GENICpossibly homozygous60850412
1129047329129047330G-3GENIChomozygous60850413
1129047336129047337GT1GENIChomozygous60850414
1129047338129047339GC1GENIChomozygous60850415
1129047353129047354AC1GENIChomozygous60850417
1129047360129047361TC4GENICheterozygous62087440
1129047361129047362CA5GENICheterozygous62087441
1129047633129047639CGCACA------10GENICheterozygous60850418
1129061038129061039TTA8GENICheterozygous60850462
1129085954129085955CCA4GENICheterozygous60850532
1129087998129087999TC13GENICheterozygous60850537
1129123707129123708AAGC2GENIChomozygous62087442
1129123708129123709TA1GENIChomozygous62087443
1129131033129131034C-11GENIChomozygous60850692
1129204496129204497TTC1INTERGENIChomozygous60850835
1129204511129204512TTC2INTERGENIChomozygous60850836
1129204516129204517GC7INTERGENICpossibly homozygous60850837
1129204607129204608TTC4INTERGENIChomozygous60850838