chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1215628833215628834AG9GENIChomozygous108534758
1215632033215632034GA23GENIChomozygous120592715
1215637319215637320GC26GENIChomozygous120592717
1215637694215637695CT22GENIChomozygous108534764
1215640556215640557AC6GENIChomozygous109056474
1215641220215641221TC16GENIChomozygous108534768
1215641965215641966GA10GENIChomozygous120592719
1215642092215642093GA19GENIChomozygous120592721
1215647075215647076CG4GENICheterozygous125492093
1215647181215647182AG14GENIChomozygous108991201
1215647295215647296GA20GENIChomozygous108991202
1215647748215647749CT8GENIChomozygous108991203
1215648350215648351CA12GENIChomozygous108534772
1215650482215650483AG21GENIChomozygous108991204
1215650660215650661CT5GENIChomozygous108991205
1215651341215651342GA9GENIChomozygous120592723
1215651461215651462GA20GENIChomozygous108991206
1215651692215651693CT16GENICheterozygous108991207
1215653364215653365AG20GENIChomozygous108991209
1215653489215653490GA17GENIChomozygous108991210
1215653676215653677TC17GENIChomozygous108991211
1215653730215653731GA5GENICheterozygous108991212
1215653752215653753GA5GENIChomozygous108991215
1215653823215653824AG16GENIChomozygous108991217
1215653957215653958AG17GENIChomozygous108991218
1215655079215655080AT9GENIChomozygous108534776
1215656968215656969CT22GENIChomozygous120592725
1215657763215657764TC15GENIChomozygous108534779
1215657771215657772GA14GENIChomozygous120592727
1215659221215659222TC19GENIChomozygous108991225
1215659387215659388CT24GENIChomozygous108534780
1215659476215659477CA19GENIChomozygous120906879