chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10106633814106633815TC27GENIChomozygous138869378
10106634338106634339AG26GENIChomozygous138869379
10106635836106635837GA24GENIChomozygous138869380
10106636162106636163CA9GENIChomozygous138869381
10106636332106636333AC25GENIChomozygous138869382
10106637133106637134TC25GENIChomozygous138869383
10106638221106638222CT14GENIChomozygous138869384
10106638273106638274TA15GENIChomozygous138869385
10106638413106638414GA17GENIChomozygous138869386
10106638507106638508GA25GENIChomozygous138869387
10106638567106638568AG24GENIChomozygous138869388
10106638881106638882TA24GENIChomozygous138869389
10106639197106639198AG16GENIChomozygous138869390
10106639379106639380CT21GENIChomozygous138869391
10106642501106642502GA20GENIChomozygous138869392
10106643792106643793AG9GENIChomozygous138869393
10106638994106638994T16GENIChomozygous138703810
10106643836106643837AC17GENICheterozygous403297288
10106643831106643832A17GENIChomozygous403297285
10106643831106643832AC17GENICheterozygous403297286
10106643836106643837A17GENIChomozygous403297287
10106643892106643893GA22GENIChomozygous138869394
10106644674106644675AT24GENIChomozygous138869395
10106648175106648176TC15GENIChomozygous138869396
10106649721106649722CT23GENIChomozygous138869397
10106649931106649932TC19GENIChomozygous138869398
10106651013106651014CT23GENIChomozygous138869399
10106651241106651242GA19GENIChomozygous138869400
10106652419106652420GA25GENIChomozygous138869401
10106653651106653652AG21GENIChomozygous138869402
10106654035106654036AG23GENIChomozygous138869403
10106654070106654071AG19GENIChomozygous138869404
10106654176106654177TG18GENIChomozygous138869405
10106654450106654451A13GENIChomozygous138703811
10106654458106654459AT13GENIChomozygous138869406
10106654502106654503CT17GENIChomozygous138869407
10106655737106655738TC20GENIChomozygous138869408
10106658823106658824TC28GENIChomozygous138869409