chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7117676507117676513TTTTTT------22GENICpossibly homozygous54078376
7117676524117676525TC25GENICpossibly homozygous54920810
7117676770117676771AG23GENIChomozygous54078377
7117677218117677219TC4GENIChomozygous54078380
7117677698117677699GGTTT22GENICheterozygous55000476
7117677698117677699GGTTTTT22GENICheterozygous55000478
7117677994117677995CA29GENIChomozygous54078384
7117678409117678410CA26GENIChomozygous54078385
7117678437117678444AATAAAT-------16GENIChomozygous54078387
7117678471117678472TC27GENIChomozygous54078388
7117679618117679619CA29GENIChomozygous54078389
7117679624117679625CT31GENIChomozygous54078390
7117680621117680622GT25GENIChomozygous54078391
7117680760117680761CT25GENIChomozygous54078392
7117680870117680871AATGTGTGTGTGTGTGTGTG6GENICheterozygous55030309
7117680870117680871AATGTGTGTGTG6GENICheterozygous55095489
7117680872117680873AG23GENIChomozygous54078393
7117681083117681084TC20GENIChomozygous54078394
7117681106117681107TG20GENIChomozygous54078395
7117681927117681928GT16GENICpossibly homozygous54078396
7117682096117682097TG22GENIChomozygous54078397
7117682127117682131GCTG----17GENIChomozygous54078398
7117682899117682900TC30GENIChomozygous54078399
7117684266117684267AG12GENIChomozygous54078400
7117684582117684612GTCCTAGTCCTAGTCCTAGTCCTAGTCCTA------------------------------14GENIChomozygous54078401
7117685326117685327AG18GENIChomozygous54078402
7117685935117685936GC30GENIChomozygous54078403
7117686292117686293CT22GENIChomozygous54078404
7117686307117686308GA21GENIChomozygous54078405
7117686432117686433AC34GENIChomozygous54078406
7117686478117686479CT31GENIChomozygous54078407
7117687040117687041AG17GENIChomozygous54078408
7117687150117687151GGC9GENIChomozygous54078409
7117687396117687397AAG10GENIChomozygous54078411
7117689399117689400CT31GENIChomozygous54078412
7117691127117691130CCG---7GENIChomozygous54078413