chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
45112807151128072T9GENIChomozygous128033703
45112807451128074A10GENIChomozygous128033704
45112807651128077GC12GENIChomozygous119276409
45112807951128080A12GENIChomozygous128033705
45112808251128082C12GENIChomozygous128033706
45112808351128084TG14GENIChomozygous119276411
45112808951128089A14GENIChomozygous128033707
45112810251128102C20GENIChomozygous128033708
45112810651128107G20GENIChomozygous128033709
45112810951128111GG21GENIChomozygous128033710
45112811151128112GA21GENIChomozygous119304574
45115771351157713G47GENIChomozygous128033737
45115975251159752A41GENIChomozygous128033740
45115976651159766AGC45GENIChomozygous128033741
45116397851163978TC19GENIChomozygous128033742
45116398051163983GGG20GENIChomozygous128033743
45116398351163984GT20GENIChomozygous119276423
45116399051163990AT23GENIChomozygous128033744
45116399151163992CG23GENIChomozygous119621884
45115955751159559TC20GENICheterozygous130929359
45116397651163977GT19GENIChomozygous112649241
45117290651172907GT5GENIChomozygous112649262
45117291151172911T6GENIChomozygous128033747
45117291351172913G6GENIChomozygous128033748
45117292151172922CG5GENIChomozygous113022904
45117292451172925T6GENIChomozygous128033749
45117292951172930C8GENIChomozygous128033750
45117293051172931CG9GENIChomozygous119276425
45117293451172935AG10GENIChomozygous113022905
45117293751172937GTA10GENIChomozygous128033751