chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1178527033178527034AG25GENIChomozygous882071732
1178527101178527102AG19GENIChomozygous882071733
1178527146178527147AG6GENIChomozygous882071734
1178527293178527294GA5GENIChomozygous882071735
1178527407178527408CT12GENIChomozygous882071736
1178527491178527492CT24GENIChomozygous882071737
1178527527178527528CT22GENIChomozygous882071738
1178527932178527933TC21GENIChomozygous882071739
1178528362178528363AG5GENIChomozygous882071740
1178528382178528383AG8GENIChomozygous882071741
1178528591178528592CT13GENIChomozygous882071742
1178528663178528664CG9GENIChomozygous882071743
1178528698178528699TA5GENIChomozygous882071744
1178528746178528747TC11GENIChomozygous882071745
1178528963178528964AG15GENIChomozygous882071746
1178530290178530291AG7GENIChomozygous882071747
1178530738178530739CA8GENICheterozygous882071748
1178531549178531550TC29GENIChomozygous882071749
1178531581178531582CT12GENIChomozygous882071750
1178531623178531624TG15GENIChomozygous882071751
1178531930178531931TC22GENIChomozygous882071752
1178533353178533354TC26GENIChomozygous882071753
1178533797178533798AG22GENIChomozygous882071754
1178534097178534098AG23GENIChomozygous882071755
1178534954178534955CG14GENIChomozygous882071756