chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
14431365944313660CCTGCT60GENICheterozygous62255657
14431366244313666ATGA----63GENICheterozygous62244505
14431369044313691CT63GENICpossibly homozygous62533357
14431372344313724AAGTGCGCG71GENICheterozygous62225960
14431372544313728CAA---73GENICheterozygous62225961
14431372944313730CT70GENIChomozygous62225962
14431373144313732GGC70GENICheterozygous62225963
14431373344313734TTTA69GENICheterozygous62225964
14431373544313736TTGGTG71GENICheterozygous62225965
14431386344313864TC69GENICheterozygous60694731
14431386844313869AC76GENICheterozygous60694732
14431388444313888TCAT----94GENICheterozygous62125740
14431387544313876TTTA82GENICheterozygous62125737
14431387844313879GA85GENICheterozygous62125738
14431388044313881AT87GENICheterozygous62125739
14431391244313913CT87GENICheterozygous61290227
14431391944313926CCCTTGT-------84GENICheterozygous60694735
14431395244313953GT83GENICheterozygous60694739
14431396344313964GT83GENICheterozygous60694740