chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1215628833215628834AG16GENIChomozygous108534758
1215632033215632034GA29GENIChomozygous120592715
1215637319215637320GC31GENICpossibly homozygous120592717
1215637694215637695CT28GENIChomozygous108534764
1215641220215641221TC20GENIChomozygous108534768
1215641965215641966GA33GENICpossibly homozygous120592719
1215642092215642093GA39GENICpossibly homozygous120592721
1215647181215647182AG24GENIChomozygous108991201
1215647295215647296GA22GENICpossibly homozygous108991202
1215647748215647749CT27GENICpossibly homozygous108991203
1215648350215648351CA16GENIChomozygous108534772
1215650482215650483AG26GENIChomozygous108991204
1215650660215650661CT16GENIChomozygous108991205
1215651341215651342GA24GENIChomozygous120592723
1215651461215651462GA27GENICpossibly homozygous108991206
1215651692215651693CT35GENICpossibly homozygous108991207
1215652832215652833GT20GENIChomozygous108991208
1215653364215653365AG33GENIChomozygous108991209
1215653489215653490GA21GENIChomozygous108991210
1215653676215653677TC22GENIChomozygous108991211
1215653730215653731GA25GENICpossibly homozygous108991212
1215653742215653743TC20GENICpossibly homozygous108991213
1215653746215653747AG22GENICpossibly homozygous108991214
1215653752215653753GA27GENICpossibly homozygous108991215
1215653754215653755GA28GENICpossibly homozygous108991216
1215653823215653824AG19GENIChomozygous108991217
1215653957215653958AG26GENICpossibly homozygous108991218
1215655079215655080AT29GENICpossibly homozygous108534776
1215655082215655083TG27GENICpossibly homozygous108534777
1215656968215656969CT16GENICpossibly homozygous120592725
1215657763215657764TC34GENICpossibly homozygous108534779
1215657771215657772GA33GENICpossibly homozygous120592727
1215659221215659222TC34GENIChomozygous108991225
1215659387215659388CT29GENICpossibly homozygous108534780