chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1181865019181865020TTACAC6GENIChomozygous60989577
1181869711181869715GTGT----13GENICpossibly homozygous60989591
1181875819181875820TC12GENIChomozygous60989603
1181880750181880754GTGT----12GENICheterozygous62180351
1181880752181880754GT--12GENICheterozygous62549368
1181891903181891904TTTCTC7GENICheterozygous62545589
1181891903181891904TTTCTCTC7GENICheterozygous62545590
1181895531181895532CCGTGTGTGTGT10GENICheterozygous62370158
1181895534181895538GTGT----10GENICheterozygous61565205
1181899551181899557GAGAGA------9GENICpossibly homozygous62545592
1181900582181900598GTTATTTTGTTTTTAG----------------21GENICheterozygous62353259
1181900873181900874C-13GENICheterozygous62180367
1181904368181904370AC--3GENICheterozygous62445037
1181906543181906544A-7GENICheterozygous60989669
1181906851181906852TC36GENIChomozygous60989671
1181918337181918338AT30GENIChomozygous60989735
1181918341181918342CG31GENIChomozygous60989737
1181918343181918344CG30GENIChomozygous60989739
1181918352181918353GA30GENIChomozygous60989741
1181918353181918354TA30GENIChomozygous60989743
1181918355181918356GA29GENIChomozygous60989745
1181884532181884533TTG10GENIChomozygous61915910
1181888266181888267A-14GENICpossibly homozygous61915911
1181888651181888652CCGTGTGT8GENIChomozygous61915912