chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104860130348601304TC24GENIChomozygous116880043
104860156148601562CT41GENIChomozygous117253399
104860225448602255GA25GENIChomozygous116880053
104860313148603132GA19GENIChomozygous117009231
104860461948604620TA19GENICheterozygous117391292
104860460048604601CT11GENICheterozygous117391286
104860461348604614TA15GENICheterozygous117391288
104860461748604618TA15GENICheterozygous117391290
104860467948604680GA28GENIChomozygous117009232
104860612348606124CA25GENIChomozygous117253401
104860689548606896CG20GENIChomozygous117253403
104861018648610187CT38GENIChomozygous117253405
104861158148611582AC5GENIChomozygous116588620
104861199148611992GA26GENIChomozygous117253407
104861307548613076GC27GENIChomozygous116880130
104861315248613153CT29GENIChomozygous117253409
104861345848613459GA23GENIChomozygous117253411
104861395448613955GA47GENIChomozygous116880137
104861591148615912CT33GENIChomozygous117253413
104861625548616256GT30GENIChomozygous117009239
104861661548616616GT28GENIChomozygous117253415
104861735848617359AG24GENIChomozygous116880154
104861756548617566GA16GENIChomozygous117253417
104861812548618126AG24GENIChomozygous116880156
104861814948618150AC21GENIChomozygous116880158
104861816548618166CT19GENIChomozygous117253419
104861816648618167AG19GENIChomozygous116880160
104861870148618702CT20GENIChomozygous116880165
104862317848623179AG27GENIChomozygous116880201
104862356048623561AG26GENIChomozygous116880207
104862512448625125CT26GENIChomozygous117253423
104862643248626433GA29GENIChomozygous117253425
104861332848613329CG27GENIChomozygous116774465