chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104892962848929629TC16GENIChomozygous116881230
104892980448929805TA23GENIChomozygous116881232
104892986348929864AG16GENIChomozygous116881234
104893001248930013AG12GENIChomozygous116881236
104893046648930467AG5GENIChomozygous116881238
104893052748930528CT11GENIChomozygous116881240
104893105348931054TC11GENIChomozygous116881242
104893119948931200AG6GENIChomozygous116881244
104893158848931589GA11GENIChomozygous117009339
104893163448931635CG4GENIChomozygous116881246
104893186348931864TC21GENIChomozygous117009340
104893229848932299GA12GENIChomozygous116881248
104893246248932463GA22GENIChomozygous116881250
104893302148933022CT8GENIChomozygous116881252
104893367948933680AG18GENIChomozygous116881254
104893417948934180TC12GENIChomozygous116881256
104893440848934409TC18GENIChomozygous116881258
104893461448934615TC18GENIChomozygous116881260
104893564248935643AG20GENIChomozygous116881264
104893608548936086GT18GENIChomozygous116881266
104893649848936499TC19GENIChomozygous116881268
104893670448936705GA5GENIChomozygous117344603
104893679148936792TC14GENIChomozygous117253623
104893700948937010AG14GENIChomozygous116881270
104893988048939881AG14GENIChomozygous116881274
104894064448940645CT8GENIChomozygous116881276
104894065948940660GC8GENIChomozygous116881278
104894067448940675GA10GENIChomozygous116881280
104894111048941111AG7GENIChomozygous117078214
104894111148941112TC7GENIChomozygous117078215
104894111948941120TG7GENIChomozygous117009348
104894162348941624AG17GENIChomozygous116881282
104894389748943898CG16GENIChomozygous116881287
104894465548944656AG15GENIChomozygous116881291
104894566448945665TC15GENIChomozygous116881299
104894571848945719GA9GENIChomozygous116881301
104894582148945822TC16GENIChomozygous117009352
104894618348946184AG18GENIChomozygous116881303
104894630248946303CA16GENIChomozygous116881305
104894709348947094CT15GENIChomozygous116881307
104894734348947344TC17GENIChomozygous116881309
104894749848947499AG6GENIChomozygous116881311