chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10106633814106633815TC18GENIChomozygous138869378
10106634338106634339AG40GENIChomozygous138869379
10106635836106635837GA39GENIChomozygous138869380
10106636162106636163CA52GENIChomozygous138869381
10106636332106636333AC32GENIChomozygous138869382
10106637133106637134TC54GENIChomozygous138869383
10106638221106638222CT36GENIChomozygous138869384
10106638273106638274TA42GENIChomozygous138869385
10106638413106638414GA51GENIChomozygous138869386
10106638507106638508GA42GENIChomozygous138869387
10106638567106638568AG44GENIChomozygous138869388
10106638881106638882TA48GENIChomozygous138869389
10106639197106639198AG32GENIChomozygous138869390
10106639379106639380CT49GENIChomozygous138869391
10106638994106638994T39GENIChomozygous138703810
10106642501106642502GA43GENIChomozygous138869392
10106644674106644675AT38GENIChomozygous138869395
10106643792106643793AG20GENIChomozygous138869393
10106643892106643893GA34GENIChomozygous138869394
10106643831106643832A26GENIChomozygous403297285
10106643831106643832AC26GENICheterozygous403297286
10106643836106643837A26GENIChomozygous403297287
10106643836106643837AC26GENICheterozygous403297288
10106648175106648176TC29GENIChomozygous138869396
10106649721106649722CT46GENIChomozygous138869397
10106649931106649932TC40GENIChomozygous138869398
10106651013106651014CT49GENIChomozygous138869399
10106651241106651242GA50GENIChomozygous138869400
10106652419106652420GA42GENIChomozygous138869401
10106653651106653652AG50GENIChomozygous138869402
10106654035106654036AG49GENIChomozygous138869403
10106654070106654071AG54GENIChomozygous138869404
10106654176106654177TG47GENICpossibly homozygous138869405
10106654450106654451A41GENIChomozygous138703811
10106654458106654459AT41GENIChomozygous138869406
10106654502106654503CT48GENIChomozygous138869407
10106655737106655738TC44GENIChomozygous138869408
10106658823106658824TC57GENIChomozygous138869409