chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104229756442297565GA11GENIChomozygous147459478
104229959442299595GA14GENIChomozygous147459479
104230004442300045AG18GENIChomozygous146953960
104230051042300511TA20GENIChomozygous146953961
104230454742304548TC12GENIChomozygous147459480
104230569142305692CA15GENIChomozygous146953963
104231137742311378GA15GENIChomozygous146953964
104231161842311619CT11GENIChomozygous146953965
104231357942313580AG16GENIChomozygous146953966
104231485642314857AC12GENIChomozygous146953967
104232171542321716CT19GENIChomozygous146953968
104232187642321877AG12GENIChomozygous147459481
104232227442322275GA14GENIChomozygous146953969
104232378642323787CT16GENIChomozygous147459482
104232418542324186AG12GENIChomozygous146953970
104232425142324252TA13GENIChomozygous147459483
104232474042324741GT10GENIChomozygous146953971
104232518042325180T13GENICheterozygous141094830
104232559142325592CG12GENIChomozygous147459484
104230437742304378AC18GENIChomozygous138776129
104232189342321897CACA12GENIChomozygous138680775
104231783542317836A11GENIChomozygous146934858
104232859642328597AC16GENICheterozygous154639881
104232859642328597A16GENIChomozygous403284535
104232927142329272GA16GENIChomozygous147459485
104233071342330714GA20GENIChomozygous146953972
104233107142331072CG10GENICheterozygous154639882
104233107142331072C10GENICpossibly homozygous403284536
104233107342331074C10GENICpossibly homozygous403634081
104233107342331074CG10GENICheterozygous403634082
104233107542331076CG10GENICheterozygous154639883
104233107542331076C10GENICpossibly homozygous403634083
104233107742331078CG10GENICpossibly homozygous154639884
104233107742331078C10GENICheterozygous403634084
104233382842333829TA17GENIChomozygous146953973
104233540942335410AG12GENIChomozygous146953974
104233982942339830AG15GENIChomozygous146953975
104234135542341359AAAG12GENIChomozygous146934861
104234135842341359GA12GENICheterozygous154641225
104234135842341359G12GENIChomozygous403634085