chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10106633814106633815TC18GENIChomozygous138869378
10106634338106634339AG20GENIChomozygous138869379
10106635836106635837GA25GENIChomozygous138869380
10106636162106636163CA19GENIChomozygous138869381
10106636332106636333AC24GENIChomozygous138869382
10106637133106637134TC17GENIChomozygous138869383
10106638221106638222CT25GENIChomozygous138869384
10106638273106638274TA26GENIChomozygous138869385
10106638413106638414GA23GENIChomozygous138869386
10106638507106638508GA29GENIChomozygous138869387
10106638567106638568AG21GENIChomozygous138869388
10106638881106638882TA19GENIChomozygous138869389
10106638994106638994T17GENIChomozygous138703810
10106639197106639198AG20GENIChomozygous138869390
10106639379106639380CT16GENIChomozygous138869391
10106642008106642008CTT5GENICheterozygous140903639
10106642501106642502GA24GENIChomozygous138869392
10106643792106643793AG10GENIChomozygous138869393
10106643831106643832A12GENIChomozygous403297285
10106643831106643832AC12GENICheterozygous403297286
10106643836106643837A12GENIChomozygous403297287
10106643836106643837AC12GENICheterozygous403297288
10106643892106643893GA20GENIChomozygous138869394
10106644674106644675AT24GENIChomozygous138869395
10106648175106648176TC13GENIChomozygous138869396
10106649721106649722CT21GENIChomozygous138869397
10106649931106649932TC26GENIChomozygous138869398
10106651013106651014CT22GENIChomozygous138869399
10106651241106651242GA23GENIChomozygous138869400
10106652419106652420GA25GENIChomozygous138869401
10106653651106653652AG24GENIChomozygous138869402
10106654035106654036AG15GENIChomozygous138869403
10106654070106654071AG16GENIChomozygous138869404
10106654176106654177TG16GENIChomozygous138869405
10106654450106654451A16GENIChomozygous138703811
10106654458106654459AT16GENIChomozygous138869406
10106654502106654503CT24GENIChomozygous138869407
10106655737106655738TC14GENIChomozygous138869408
10106658823106658824TC27GENIChomozygous138869409