chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103856141638561419AGC---16GENIChomozygous752504789
103856179638561797CT27GENIChomozygous642348442
103856193738561938AG24GENIChomozygous642348443
103856233238562333AC26GENIChomozygous642348444
103856237438562375CG19GENIChomozygous642348445
103856247838562479CA24GENIChomozygous642348446
103856272138562725GTGC----13GENIChomozygous752504790
103856282538562826TC23GENIChomozygous642348447
103856290738562908TTTTTA15GENIChomozygous752504791
103856298038562981TC18GENIChomozygous642348448
103856307238563073CT24GENICpossibly homozygous642348449
103856318138563182AG25GENIChomozygous642348450
103856323638563237AC26GENIChomozygous642348451
103856332638563327GA30GENIChomozygous642348452
103856344238563443AG45GENIChomozygous642348453
103856365538563656CCAG25GENIChomozygous752504792
103856382938563830CT32GENIChomozygous642348454
103856391038563912AA--19GENIChomozygous752504793
103856420238564203GGAAA18GENICheterozygous752504794
103856421238564213AAG22GENICheterozygous752504795
103856424338564244CG11GENIChomozygous642348455
103856438538564386AG20GENIChomozygous642348456
103856466438564665GA20GENIChomozygous642348457
103856470538564706TTC22GENIChomozygous752504796