chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103856179638561797CT23GENICheterozygous52042986
103856193738561938AG18GENIChomozygous51853062
103856233238562333AC23GENIChomozygous51853065
103856237438562375CG18GENIChomozygous51853068
103856247838562479CA22GENIChomozygous51853071
103856270538562706TTTGTGTGTG10GENICheterozygous52369215
103856282538562826TC24GENIChomozygous51853079
103856290738562908TTTTTA14GENIChomozygous51853082
103856298038562981TC20GENIChomozygous51853084
103856307238563073CT18GENICheterozygous52042988
103856318138563182AG23GENIChomozygous51853087
103856323638563237AC26GENIChomozygous51853090
103856332638563327GA16GENICheterozygous52042990
103856344238563443AG15GENIChomozygous51853093
103856365538563656CCAG13GENICheterozygous52042992
103856382938563830CT23GENIChomozygous51853096
103856391038563912AA--11GENIChomozygous51853100
103856424338564244CG12GENICheterozygous52043000
103856438538564386AG11GENIChomozygous51853109
103856466438564665GA9GENICheterozygous52043002
103856470538564706TTC14GENIChomozygous51853112
103856272438562725CT9GENICheterozygous52316408
103856272138562725GTGC----13GENICheterozygous51985044