chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
186068656060686561CG39GENIChomozygous46479963
186068658660686587AT32GENIChomozygous46479964
186068689760686898AATTTTT21GENIChomozygous46479965
186068690260686903TTTTTTC22GENICpossibly homozygous46479966
186068719060687191GGC9GENIChomozygous46665791
186068747860687479CT20GENIChomozygous46479967
186068751260687513CCT15GENIChomozygous46479968
186068752660687527TTTC18GENICpossibly homozygous46479969
186068757560687576CT16GENIChomozygous46479970
186068761360687614CT16GENIChomozygous46479971
186068781560687816CT25GENIChomozygous46479972
186068788060687881CT14GENIChomozygous46479973
186068789960687900TC15GENIChomozygous46479974
186068794060687941CCT11GENIChomozygous46479975
186068797360687974TC14GENIChomozygous46479976
186068806160688062AC15GENIChomozygous46479977
186068830260688303TC24GENIChomozygous46479979
186068839560688396CT23GENIChomozygous46479980
186068869560688696TA21GENIChomozygous46665792
186068880560688806GA18GENIChomozygous46479981
186068884060688841A-17GENIChomozygous46665793
186068912060689121GT20GENIChomozygous46689386
186068965160689652CT26GENIChomozygous46689387
186069024260690243TC16GENICpossibly homozygous46479983
186069061060690611CT18GENIChomozygous46479984
186069140760691408GA28GENIChomozygous46665795
186069227660692277TG35GENIChomozygous46479986
186069292060692934AAAAAAAAAAAAAA--------------6GENICheterozygous46479987
186069292160692934AAAAAAAAAAAAA-------------6GENICheterozygous46479988
186069308160693082AG25GENIChomozygous46479989
186069364760693648GA37GENIChomozygous46665797
186069726060697261TG30GENIChomozygous46479997
186069445560694456GGC26GENIChomozygous46665798
186069467160694672CA16GENIChomozygous46479990
186069509860695099AG16GENIChomozygous46479992
186069711060697111GT22GENIChomozygous46479996
186069749460697495AG23GENIChomozygous46479998
186069756460697565TC22GENIChomozygous46665801
186069861060698611TC19GENIChomozygous46480000
186070060460700605CT14GENIChomozygous46689388
186070130760701308GT36GENIChomozygous46689389
186070190060701901AC21GENICpossibly homozygous46480008
186070240660702407AG18GENIChomozygous46480009
186070246960702470TC15GENIChomozygous46480011