chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121124228311242284AG12GENIChomozygous115415349
121124230011242301GA11GENIChomozygous115361396
121124304311243044GA13GENIChomozygous115415351
121124305411243055AC17GENIChomozygous115415353
121124389311243894TG21GENIChomozygous115254912
121124392111243922TG27GENIChomozygous115415355
121124435311244354TC13GENIChomozygous115415357
121124442511244426CA22GENIChomozygous115415359
121124456111244562CT11GENIChomozygous115415361
121124456511244566CT10GENIChomozygous115415363
121124477311244774TC7GENIChomozygous115445087
121124483411244835GA9GENIChomozygous115361397
121124484011244841GA9GENIChomozygous115415365
121124486711244868TC9GENIChomozygous115415367
121124545811245459CT20GENIChomozygous115415369
121124554511245546CT24GENIChomozygous115415371
121124562311245624AG6GENIChomozygous115415373
121124581911245820AT21GENIChomozygous115415375
121124666611246667GA26GENIChomozygous115415377
121124682111246822GA9GENIChomozygous115254916
121124691611246917GC7GENIChomozygous118244404
121124858011248581AG9GENIChomozygous115415379
121124958211249583CT7GENICheterozygous115594779
121124990211249903AT26GENIChomozygous115415381
121124804111248042TG16GENIChomozygous126220312
121124804711248048GT6GENICheterozygous126220313
121124936111249362TG4GENICheterozygous126220314
121124804811248049GT9GENIChomozygous115653331