chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
17244385272443853CT13GENICheterozygous108865899
17244392772443928TC4GENIChomozygous108865900
17244401572444016CT5GENIChomozygous109106318
17244424272444243TG15GENIChomozygous108865901
17244528672445287TC14GENIChomozygous108865903
17244581372445814CT9GENIChomozygous109106320
17244603272446033CT18GENIChomozygous108865904
17244736572447366CA10GENIChomozygous108865910
17244751672447517AG14GENIChomozygous108865911
17244933572449336TC7GENICheterozygous109106324
17245063472450635CA17GENIChomozygous109106328
17245081572450816GA21GENIChomozygous109106330
17245157172451572AG12GENIChomozygous108865932
17245229672452297TC13GENIChomozygous109106332
17245234372452344CT14GENIChomozygous109106334
17245489072454891GA27GENIChomozygous109106336
17245652672456527GC25GENIChomozygous108865937
17245678272456783GA20GENIChomozygous108865939
17245742372457424GT12GENIChomozygous108865942
17245756772457568GA20GENIChomozygous109106338
17245846572458466TA18GENIChomozygous108865943
17245912672459127TG23GENIChomozygous108865946
17246006572460066GT20GENIChomozygous108865947
17246038172460382GA5GENIChomozygous109106340
17246046672460467GA11GENIChomozygous109106342
17246048172460482GA10GENIChomozygous109106344
17246140472461405AG7GENIChomozygous108865950
17245005572450056CT8GENIChomozygous125427015