chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8117047649117047650TC21GENIChomozygous634894753
8117047707117047708GGA12GENIChomozygous747727074
8117047711117047719AAAAAAAA--------4GENICheterozygous747727075
8117047712117047719AAAAAAA-------4GENICheterozygous747727076
8117051665117051666TA35GENIChomozygous634894754
8117051666117051667AG35GENIChomozygous634894755
8117052068117052069AG21GENIChomozygous634894756
8117052890117052891AG30GENIChomozygous634894757
8117053416117053417AG28GENIChomozygous634894758
8117054122117054123CT17GENIChomozygous634894759
8117054158117054159AG23GENIChomozygous634894760
8117054572117054573CCTT1GENIChomozygous747727077
8117055369117055370TC41GENIChomozygous634894761
8117058726117058727CT24GENIChomozygous634894762
8117060845117060846CCCT12GENIChomozygous747727078
8117060960117060961GA19GENIChomozygous634894763
8117062340117062341TTGTCA22GENIChomozygous747727079
8117065011117065012AG23GENIChomozygous634894764
8117066348117066349CT32GENIChomozygous634894765
8117066426117066427GA32GENIChomozygous634894766
8117067190117067191GGCTGT24GENIChomozygous747727080
8117067250117067251AG29GENIChomozygous634894767
8117067587117067588TC18GENIChomozygous634894768
8117068570117068571TC24GENIChomozygous634894769
8117068680117068681CA19GENIChomozygous634894770
8117068800117068801AG22GENIChomozygous634894771
8117068936117068937TTTC9GENIChomozygous747727081
8117069221117069222GA7GENIChomozygous634894772
8117069252117069253CG5GENIChomozygous634894773
8117069273117069291CAACCACATGGTGGCTCA------------------2GENIChomozygous747727082
8117069378117069379TTAA7GENIChomozygous747727084
8117069479117069480CCA2GENICheterozygous747727085
8117069479117069480CCAA2GENICheterozygous747727086
8117070028117070029TC16GENIChomozygous634894774
8117070419117070420GT29GENIChomozygous634894775
8117070774117070775TA7GENIChomozygous634894776
8117071534117071535CT22GENIChomozygous634894777
8117071896117071897GA29GENIChomozygous634894778
8117072006117072007CT23GENIChomozygous634894779
8117072252117072253AAG33GENICpossibly homozygous747727088
8117072502117072503TC21GENIChomozygous634894780
8117072674117072675AATG29GENICpossibly homozygous747727089
8117072705117072706AAGT33GENIChomozygous747727090
8117072721117072722AAGT41GENIChomozygous747727091
8117072752117072754GT--40GENICpossibly homozygous747727092
8117072978117072979AG24GENIChomozygous634894781
8117074092117074093TC27GENIChomozygous634894782
8117074214117074215AG22GENIChomozygous634894783
8117074602117074603GA21GENIChomozygous634894784
8117074807117074808CA25GENIChomozygous634894785
8117074996117074997AG24GENIChomozygous634894786
8117075165117075166AG10GENIChomozygous634894787
8117075471117075472GA20GENIChomozygous634894788
8117075695117075696GA24GENIChomozygous634894789
8117075829117075830TC22GENIChomozygous634894790
8117076754117076755CT30GENIChomozygous634894791
8117077840117077841CT22GENIChomozygous634894792
8117078068117078069CCTTTTTTCTTTTTTT11GENICheterozygous747727093
8117078068117078069CCTTTTTTCTTTTTTTT11GENICheterozygous747727094
8117078122117078123GC19GENIChomozygous634894793
8117078125117078131AGCGCT------20GENIChomozygous747727095