chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
726154382615439CT59GENIChomozygous53765963
726154742615475CT58GENICpossibly homozygous53765964
726157322615733CT60GENIChomozygous53765966
726161502616152CC--12GENICheterozygous53765968
726161602616162CT--8GENIChomozygous53765969
726161612616162T-12GENIChomozygous53765971
726178512617852GA33GENIChomozygous53765972
726181452618146CT36GENIChomozygous53765974
726189032618904CCT23GENICpossibly homozygous53765975
726189142618915AT29GENIChomozygous53765977
726189192618920AG30GENIChomozygous53765979
726191592619160CCT4GENIChomozygous53765980
726194602619461TA39GENIChomozygous53765982
726195772619590GTATAGGTGTTTA-------------28GENIChomozygous53765984
726197902619792TT--16GENICheterozygous53765985
726197912619792T-16GENICpossibly homozygous53765987
726199662619967GA63GENIChomozygous53765989
726204652620466CT46GENIChomozygous53765990
726209922620993CCT19GENICpossibly homozygous53765992
726209952620996TTC23GENIChomozygous53765994
726215152621517TT--3GENICheterozygous53765995
726215162621517T-3GENICheterozygous53765997