chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
97384104773841048CT19GENICheterozygous52018344
97385359473853595CA33GENICheterozygous52018475
97385735173857352CT37GENICheterozygous52235754
97385737373857374AG43GENICheterozygous52018512
97386635973866360GC45GENICheterozygous52235769
97386699273866993TTA31GENICheterozygous52235770
97386768773867688GT28GENICheterozygous52235773
97387053473870535CT31GENICheterozygous52235774
97387263873872639TG16GENICheterozygous52018561
97388818273888183GA18GENICheterozygous52018635
97390115973901164AGGCC-----16GENICheterozygous52018715
97391347573913476TC17GENICheterozygous52018748
97391918773919188GT27GENICheterozygous52018775
97392292473922925TG29GENICheterozygous52018796
97392318773923188GGA19GENICheterozygous52018797
97394058773940588GA38GENICheterozygous52018884
97404517074045171AT13GENICheterozygous52235841
97404553574045536AAG15GENICheterozygous52235842
97404557774045578AG16GENICheterozygous52019223
97405034274050343GA12GENICheterozygous52235850
97407076174070762GA15GENICheterozygous52019323
97408205174082053AG--22GENICheterozygous52235865
97409188774091888GC7GENICheterozygous52235886
97409194574091946CT13GENICheterozygous52235887
97409196274091963AG11GENICheterozygous52235888