chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7117676507117676513TTTTTT------12GENIChomozygous54078376
7117676524117676525TC16GENIChomozygous54920810
7117676770117676771AG20GENIChomozygous54078377
7117677205117677206T-4GENIChomozygous54078378
7117677210117677211TTG2GENIChomozygous55000474
7117677218117677219TC2GENIChomozygous54078380
7117677698117677699GGTTT4GENICheterozygous55000476
7117677698117677699GGTTTTT4GENICheterozygous55000478
7117677994117677995CA10GENIChomozygous54078384
7117678409117678410CA5GENIChomozygous54078385
7117678437117678444AATAAAT-------1GENIChomozygous54078387
7117678471117678472TC11GENIChomozygous54078388
7117679618117679619CA15GENIChomozygous54078389
7117679624117679625CT16GENIChomozygous54078390
7117680621117680622GT19GENIChomozygous54078391
7117680760117680761CT14GENIChomozygous54078392
7117680870117680871AATGTGTGTGTGTGTG1GENIChomozygous55000480
7117680872117680873AG10GENIChomozygous54078393
7117681083117681084TC15GENIChomozygous54078394
7117681106117681107TG17GENIChomozygous54078395
7117681927117681928GT14GENIChomozygous54078396
7117682096117682097TG12GENIChomozygous54078397
7117682127117682131GCTG----7GENIChomozygous54078398
7117682899117682900TC17GENIChomozygous54078399
7117684266117684267AG10GENIChomozygous54078400
7117684582117684612GTCCTAGTCCTAGTCCTAGTCCTAGTCCTA------------------------------14GENIChomozygous54078401
7117685326117685327AG15GENIChomozygous54078402
7117685935117685936GC19GENIChomozygous54078403
7117686292117686293CT4GENIChomozygous54078404
7117686307117686308GA7GENIChomozygous54078405
7117686432117686433AC15GENIChomozygous54078406
7117686478117686479CT12GENIChomozygous54078407
7117687040117687041AG9GENIChomozygous54078408
7117687150117687151GGC1GENIChomozygous54078409
7117687396117687397AAG3GENIChomozygous54078411
7117689399117689400CT15GENIChomozygous54078412
7117691127117691130CCG---3GENIChomozygous54078413