chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7117676507117676513TTTTTT------12GENIChomozygous54078376
7117676524117676525TC14GENIChomozygous54920810
7117676770117676771AG24GENIChomozygous54078377
7117677698117677699GGTTT7GENICheterozygous55000476
7117677698117677699GGTTTTT7GENICheterozygous55000478
7117677994117677995CA17GENIChomozygous54078384
7117678409117678410CA17GENIChomozygous54078385
7117678437117678444AATAAAT-------9GENIChomozygous54078387
7117678471117678472TC21GENIChomozygous54078388
7117679618117679619CA16GENIChomozygous54078389
7117679624117679625CT16GENIChomozygous54078390
7117680621117680622GT22GENICpossibly homozygous54078391
7117680760117680761CT24GENIChomozygous54078392
7117680870117680871AATGTGTGTGTG7GENIChomozygous55095489
7117680872117680873AG16GENIChomozygous54078393
7117681083117681084TC13GENIChomozygous54078394
7117681106117681107TG15GENIChomozygous54078395
7117681927117681928GT21GENIChomozygous54078396
7117682096117682097TG13GENIChomozygous54078397
7117682127117682131GCTG----14GENIChomozygous54078398
7117682899117682900TC15GENIChomozygous54078399
7117684266117684267AG11GENIChomozygous54078400
7117684582117684612GTCCTAGTCCTAGTCCTAGTCCTAGTCCTA------------------------------13GENIChomozygous54078401
7117685326117685327AG14GENIChomozygous54078402
7117685935117685936GC19GENIChomozygous54078403
7117686292117686293CT11GENIChomozygous54078404
7117686307117686308GA15GENIChomozygous54078405
7117686432117686433AC16GENIChomozygous54078406
7117686478117686479CT19GENIChomozygous54078407
7117687040117687041AG19GENIChomozygous54078408
7117687150117687151GGC9GENIChomozygous54078409
7117687396117687397AAG6GENIChomozygous54078411
7117689399117689400CT24GENIChomozygous54078412