chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1811457541145755CT22GENIChomozygous110568911
1811475241147525GA19GENIChomozygous110512406
1811492351149236GA22GENIChomozygous110512408
1811502121150213GA21GENIChomozygous119577900
1811502151150216AG21GENIChomozygous119577901
1811507411150742CT22GENIChomozygous110568915
1811518001151801TC20GENIChomozygous110568922
1811518181151819TC18GENIChomozygous110568925
1811502141150215AT21GENIChomozygous119509952
1811502231150224TC20GENIChomozygous119509954
1811502441150245GT18GENIChomozygous119509956
1811531121153113AG22GENIChomozygous110640989
1811540811154082CT15GENIChomozygous110512410
1811541971154198GA15GENIChomozygous110568930
1811577711157772AC18GENIChomozygous110512415
1811599241159925CT18GENIChomozygous110512419
1811612741161275GA19GENIChomozygous110512422
1811642541164255TA20GENIChomozygous110568935
1811635941163595CT23GENIChomozygous110670167
1811640081164009CT23GENIChomozygous110670169
1811662531166254GA20GENIChomozygous110670171
1811662901166291GA11GENIChomozygous110512426
1811665731166574TC16GENIChomozygous119509958
1811667951166796CT18GENIChomozygous119509962
1811668301166831TC14GENIChomozygous119509966
1811670801167081TA21GENIChomozygous110670173
1811682841168285GT26GENIChomozygous110512428
1811704901170491TG19GENIChomozygous110512430
1811726371172638GA22GENIChomozygous110512432
1811707791170780T19GENIChomozygous131754991
1811532231153223TAATCT16GENIChomozygous131202381
1811550321155033T11GENIChomozygous131202382
1811752231175223TTTCAGA26GENIChomozygous131202386