chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7117676507117676513TTTTTT------11GENICpossibly homozygous54078376
7117676770117676771AG28GENIChomozygous54078377
7117677205117677206T-2GENIChomozygous54078378
7117677209117677211GT--3GENIChomozygous54078379
7117677218117677219TC2GENIChomozygous54078380
7117677721117677722CT20GENICheterozygous54078381
7117677726117677727CT20GENICheterozygous54078382
7117677726117677727CCT13GENICpossibly homozygous54078383
7117677994117677995CA27GENIChomozygous54078384
7117678409117678410CA3GENICheterozygous54078385
7117678431117678432CCA2GENIChomozygous54078386
7117678437117678444AATAAAT-------3GENIChomozygous54078387
7117678471117678472TC6GENIChomozygous54078388
7117679618117679619CA39GENIChomozygous54078389
7117679624117679625CT39GENICpossibly homozygous54078390
7117680621117680622GT36GENIChomozygous54078391
7117680760117680761CT38GENIChomozygous54078392
7117680870117680871AG32GENICheterozygous54507448
7117680872117680873AG34GENICpossibly homozygous54078393
7117681083117681084TC40GENIChomozygous54078394
7117681106117681107TG42GENIChomozygous54078395
7117681927117681928GT31GENIChomozygous54078396
7117682096117682097TG30GENIChomozygous54078397
7117682127117682131GCTG----24GENIChomozygous54078398
7117682899117682900TC48GENICpossibly homozygous54078399
7117684266117684267AG35GENIChomozygous54078400
7117684582117684612GTCCTAGTCCTAGTCCTAGTCCTAGTCCTA------------------------------7GENIChomozygous54078401
7117685326117685327AG24GENIChomozygous54078402
7117685935117685936GC30GENIChomozygous54078403
7117686292117686293CT36GENIChomozygous54078404
7117686307117686308GA31GENIChomozygous54078405
7117686432117686433AC33GENIChomozygous54078406
7117686478117686479CT36GENIChomozygous54078407
7117687040117687041AG16GENIChomozygous54078408
7117687150117687151GGC26GENIChomozygous54078409
7117689399117689400CT31GENIChomozygous54078412
7117691127117691130CCG---21GENIChomozygous54078413