chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1256883101256883102CT28GENIChomozygous108622924
1256883224256883225AC10GENIChomozygous108622925
1256884336256884337GA15GENIChomozygous108622926
1256884942256884943TC24GENIChomozygous108622927
1256885019256885020AG20GENIChomozygous108622928
1256885728256885729CT14GENIChomozygous108622929
1256886336256886337AG27GENIChomozygous108622930
1256887880256887881AG19GENIChomozygous108622934
1256888223256888224CT14GENIChomozygous108622935
1256888267256888268CA16GENIChomozygous108622936
1256888683256888684CT11GENIChomozygous108622938
1256889954256889955CT19GENIChomozygous108622940
1256891341256891342GA22GENIChomozygous108622941
1256892358256892359CT15GENIChomozygous108622942
1256893917256893918GC17GENIChomozygous108622943
1256893928256893929GA12GENIChomozygous108622944
1256894495256894496TC16GENICheterozygous108622946
1256894569256894570AC11GENIChomozygous108622947
1256896922256896923TG21GENIChomozygous108622948
1256897044256897045CT15GENIChomozygous108622949
1256897325256897326AG10GENIChomozygous108622950
1256903853256903854TC4GENIChomozygous108622953
1256906515256906516GA13GENIChomozygous108622955
1256908033256908034TC11GENIChomozygous108622956
1256912034256912035GC17GENIChomozygous108622959