chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1221910318221910319CT12GENICheterozygous144572636
1221926000221926001T20GENICpossibly homozygous403879740
1221926000221926001TG20GENICheterozygous403879741
1222016290222016291T19GENIChomozygous403548506
1222016290222016291TC19GENICheterozygous403548507
1222025650222025651GC31GENICheterozygous143813410
1221973586221973586TATCTATG16GENICheterozygous135461598
1221988470221988471T10GENICpossibly homozygous402980451
1221988470221988471TG10GENICheterozygous402980452
1221988473221988474TC10GENICpossibly homozygous135815535
1221988481221988482TC18GENIChomozygous135815536
1221988901221988901A40GENICheterozygous144529688
1222110851222110852A14GENICheterozygous403548510
1222110851222110852AT14GENICheterozygous403548511
1222153760222153761AC37GENICheterozygous402980454
1222153760222153761A37GENICheterozygous402980455
1222165837222165839AC29GENICheterozygous141180416