chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7117676524117676525TC1GENIChomozygous54920810
7117676770117676771AG13GENICpossibly homozygous54078377
7117677994117677995CA13GENIChomozygous54078384
7117678471117678472TC2GENIChomozygous54078388
7117679618117679619CA8GENICpossibly homozygous54078389
7117679624117679625CT8GENIChomozygous54078390
7117680621117680622GT19GENIChomozygous54078391
7117680760117680761CT29GENIChomozygous54078392
7117681083117681084TC18GENICheterozygous54078394
7117681106117681107TG23GENIChomozygous54078395
7117681927117681928GT12GENICpossibly homozygous54078396
7117682096117682097TG16GENICheterozygous54078397
7117682127117682131GCTG----4GENIChomozygous54078398
7117682899117682900TC21GENICpossibly homozygous54078399
7117684266117684267AG8GENICpossibly homozygous54078400
7117685326117685327AG19GENICpossibly homozygous54078402
7117685935117685936GC15GENICpossibly homozygous54078403
7117686292117686293CT18GENICpossibly homozygous54078404
7117686307117686308GA14GENIChomozygous54078405
7117686432117686433AC12GENICheterozygous54078406
7117686478117686479CT24GENICpossibly homozygous54078407
7117687040117687041AG14GENIChomozygous54078408
7117687150117687151GGC4GENIChomozygous54078409
7117689399117689400CT22GENICpossibly homozygous54078412
7117691127117691130CCG---2GENIChomozygous54078413