chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
97384104773841048CT18GENICheterozygous52018344
97385359473853595CA31GENICheterozygous52018475
97385735173857352CT47GENICheterozygous52235754
97385737373857374AG50GENICheterozygous52018512
97386635973866360GC30GENICheterozygous52235769
97386699273866993TTA36GENICheterozygous52235770
97386768773867688GT35GENICheterozygous52235773
97387053473870535CT36GENICheterozygous52235774
97387263873872639TG22GENICheterozygous52018561
97388818273888183GA17GENICheterozygous52018635
97390115973901164AGGCC-----15GENICheterozygous52018715
97391347573913476TC21GENICheterozygous52018748
97391918773919188GT27GENICheterozygous52018775
97392292473922925TG29GENICheterozygous52018796
97392318773923188GGA33GENICheterozygous52018797
97394058773940588GA19GENICheterozygous52018884
97404517074045171AT13GENICheterozygous52235841
97404553574045536AAG18GENICheterozygous52235842
97404557774045578AG23GENICheterozygous52019223
97405034274050343GA13GENICheterozygous52235850
97407076174070762GA11GENICheterozygous52019323
97408205174082053AG--18GENICheterozygous52235865
97409188774091888GC10GENICheterozygous52235886
97409194574091946CT22GENICheterozygous52235887
97409196274091963AG22GENICheterozygous52235888