chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
107392858973928590TTG4GENICheterozygous52566123
107392965273929653TC27GENIChomozygous51495326
107393074573930746TC38GENIChomozygous51495333
107393097473930975GT26GENIChomozygous52321223
107393300073933001TTTGA22GENIChomozygous51495340
107393305573933056AG21GENIChomozygous51495342
107393348673933487TC19GENIChomozygous51495345
107393393373933934CA8GENIChomozygous51495349
107393395173933952GC5GENICheterozygous52321225
107393422173934222TC20GENIChomozygous52566126
107393479473934795GT36GENIChomozygous52727666
107393804073938041TTG21GENIChomozygous52727668
107393955873939559TTACACACAC4GENICheterozygous52504410
107393955873939559TTACACACACAC4GENICheterozygous52504412
107393980373939804GT31GENIChomozygous52727670
107394038073940381TTG27GENIChomozygous51495389
107394255173942552GGT12GENIChomozygous52727672
107394255273942553GGTGTGT12GENIChomozygous53028007
107394259373942594AG21GENIChomozygous52727676
107394260173942602GGCGCGC21GENIChomozygous52727678
107394260273942603TTC23GENIChomozygous52727680
107394334873943349TC20GENIChomozygous51495396
107394527673945277TC33GENIChomozygous51495405
107394551473945515AT28GENIChomozygous52996478
107394869373948694TC12GENIChomozygous51495414
107395324673953247GGA13GENICpossibly homozygous51695705
107395482473954825TC31GENIChomozygous51495424
107395489173954892GT17GENIChomozygous51495425
107395641873956419CT25GENIChomozygous51495428
107395794473957945GGCCAGCC19GENIChomozygous52385805
107395794773957952TTTTT-----21GENIChomozygous52385807