chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1222420529222420530GA16GENICheterozygous598214333
1222422917222422919GG--4GENIChomozygous726392223
1222423658222423659GC17GENICpossibly homozygous598214334
1222423822222423823AG26GENICheterozygous596191532
1222424140222424141TA24GENICpossibly homozygous596191533
1222424166222424167GA22GENICpossibly homozygous596191534
1222424496222424497CT35GENICpossibly homozygous598214335
1222424847222424848TC29GENICpossibly homozygous598214336
1222424952222424953AAT10GENICpossibly homozygous726392224
1222425380222425381CT9GENIChomozygous596191535
1222425570222425571TC19GENIChomozygous596191536
1222425770222425771TC10GENICpossibly homozygous596191537
1222426261222426262CA21GENICpossibly homozygous598214337
1222426669222426670TC32GENICpossibly homozygous598214338
1222427408222427409GA20GENIChomozygous596191538
1222427544222427545AG26GENIChomozygous598214339
1222428014222428015AG27GENIChomozygous598214340
1222428174222428175AG34GENIChomozygous598214341
1222429285222429286CT11GENICpossibly homozygous598214342
1222431706222431707AG24GENIChomozygous596191539
1222433540222433541CT15GENIChomozygous598214343
1222434132222434133TC9GENICpossibly homozygous596191540
1222434321222434322TC27GENICpossibly homozygous598214344