chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103856141638561419AGC---33GENIChomozygous759303693
103856179638561797CT36GENIChomozygous653755304
103856193738561938AG21GENIChomozygous653755305
103856233238562333AC18GENIChomozygous653755306
103856237438562375CG28GENIChomozygous653755307
103856247838562479CA27GENIChomozygous653755308
103856272138562725GTGC----20GENIChomozygous759303694
103856282538562826TC14GENIChomozygous653755309
103856290738562908TTTTTA19GENIChomozygous759303695
103856298038562981TC31GENIChomozygous653755310
103856307238563073CT19GENIChomozygous653755311
103856318138563182AG30GENIChomozygous653755312
103856323638563237AC25GENIChomozygous653755313
103856332638563327GA29GENIChomozygous653755314
103856344238563443AG29GENIChomozygous653755315
103856365538563656CCAG22GENIChomozygous759303696
103856382938563830CT27GENIChomozygous653755316
103856391038563912AA--15GENIChomozygous759303697
103856421238564213AAG25GENIChomozygous759303698
103856424338564244CG24GENIChomozygous653755317
103856438538564386AG28GENIChomozygous653755318
103856466438564665GA26GENIChomozygous653755319
103856470538564706TTC30GENIChomozygous759303699