chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124905051449050515TTC12GENIChomozygous50230908
124905051549050516TTTTC5GENIChomozygous50230910
124905051949050520AC13GENIChomozygous50575612
124905052349050524AC13GENIChomozygous50230912
124905052749050528AC13GENIChomozygous50230914
124905053149050532AC16GENIChomozygous50230916
124905053549050536AC15GENIChomozygous50230918
124905053949050540AC15GENIChomozygous50230920
124905054349050544AC15GENIChomozygous50230922
124905175549051756GGT4GENICheterozygous50546601
124905176049051761T-4GENICheterozygous50559366
124905205549052056C-4GENICheterozygous50546603
124905230149052313GTGTGTGTGAGT------------31GENIChomozygous50827981
124905236449052365AT41GENIChomozygous50230932
124905276849052769TC31GENIChomozygous50230934
124905276949052770GC33GENIChomozygous50827983
124905572249055723TG2GENIChomozygous50513695
124905571649055717TTG1GENIChomozygous50343654