chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108615860186158602GT17GENIChomozygous116815995
108615916686159167AG15GENIChomozygous116667272
108616461586164616TG17GENICheterozygous116815997
108616916886169169AG19GENIChomozygous116667278
108616958186169582TC31GENIChomozygous116667280
108616983386169834CT32GENIChomozygous116667282
108617278386172784GT17GENIChomozygous116816001
108617368086173681CG27GENIChomozygous116816003
108617883486178835TC16GENIChomozygous116667294
108618131086181311CT23GENIChomozygous117197577
108618151886181519AG27GENIChomozygous116816007
108618575586185756CG26GENIChomozygous116816009
108618582486185825AG12GENIChomozygous116667306
108618643686186437TC17GENIChomozygous117197579
108618789586187896AT26GENIChomozygous116667308
108618884486188845AG13GENIChomozygous116667310
108619038086190381CA12GENIChomozygous116816011
108619221886192219CT17GENIChomozygous116816013
108619352686193527AC27GENIChomozygous116816015
108619448286194483AG17GENIChomozygous116667312
108619476886194769AG20GENIChomozygous116816017
108619596886195969GC30GENIChomozygous116816019
108619619786196198TC19GENIChomozygous116816021
108619653986196540TA15GENIChomozygous116816023
108620227486202275AG27GENIChomozygous116816027
108620755386207554GA21GENIChomozygous116667322
108620769086207691TC19GENIChomozygous116816029
108621047286210473TC26GENIChomozygous116816031