chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
18131501681315017TC12GENIChomozygous61882190
18131586781315868TC14GENIChomozygous62686672
18131600181316002GGAA14GENICheterozygous61882193
18131600181316002GGAAA14GENICheterozygous62445848
18131658881316589TC10GENIChomozygous61882195
18131759681317597GA15GENIChomozygous62686673
18131777981317780CT22GENIChomozygous62686674
18131782681317827TC19GENICpossibly homozygous62686675
18131784081317841CT19GENIChomozygous62686676
18131847081318471GGAAAA5GENICheterozygous62227852
18131847781318478G-12GENICheterozygous62136212
18131847781318478GGAAAAAAAA10GENICheterozygous62136213
18131952281319523CCTTTT5GENICheterozygous62136215
18132001981320020GA22GENIChomozygous62686677
18132005481320055CA18GENIChomozygous61882200
18132072581320726CT19GENIChomozygous62686678
18132098781320988CCAAAA14GENIChomozygous62136216
18132144281321443GA8GENIChomozygous62686679
18132171681321717TTTC10GENIChomozygous62686680
18132173381321734CA13GENIChomozygous62686681
18132350381323504CG8GENIChomozygous61882205
18131952281319523CCTTT5GENICheterozygous61726702
18132241981322420AC12GENIChomozygous60746665