chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
13101474909101474910GA8GENIChomozygous66380624
13101475052101475053CT8GENIChomozygous66380626
13101476216101476217CA14GENIChomozygous66168221
13101476217101476218CG14GENIChomozygous66168224
13101476218101476219CG14GENIChomozygous66168227
13101476219101476220CG14GENIChomozygous66168230
13101476220101476221CT14GENIChomozygous66168233
13101476740101476741TC29GENIChomozygous66380628
13101477128101477129CT31GENIChomozygous66380630
13101477395101477396AT36GENIChomozygous66380632
13101477463101477464GA40GENIChomozygous66380634
13101477549101477550CT22GENIChomozygous66380636
13101487413101487414CT22GENICpossibly homozygous66380638
13101487884101487885TC5GENICheterozygous67649733
13101487908101487909TC7GENIChomozygous66380652
13101488040101488041CT22GENICheterozygous66380670
13101488049101488050CT20GENICheterozygous66168245
13101488208101488209TC12GENICheterozygous66380684
13101488211101488212CT12GENICheterozygous66380686
13101488418101488419TC18GENIChomozygous66380688
13101488426101488427TC16GENIChomozygous66380690
13101488486101488487GA19GENIChomozygous66380692
13101488658101488659TC15GENIChomozygous66380694
13101488973101488974AG28GENIChomozygous66380696
13101489548101489549CT21GENIChomozygous66380700
13101489573101489574TC28GENIChomozygous66380702
13101489615101489616TG22GENIChomozygous66380704
13101489634101489635TC28GENIChomozygous66380706
13101489734101489735CT15GENIChomozygous66380708
13101489755101489756CT18GENIChomozygous66380710
13101489857101489858AG21GENIChomozygous66380712
13101490475101490476GA40GENIChomozygous66380714
13101490482101490483GA37GENIChomozygous66380716
13101491894101491895GA32GENIChomozygous66380718
13101492130101492131AG25GENIChomozygous66380720