chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
45112807151128072T8GENIChomozygous128033703
45112807451128074A9GENIChomozygous128033704
45112807651128077GC9GENIChomozygous119276409
45112807951128080A10GENIChomozygous128033705
45112808251128082C11GENIChomozygous128033706
45112808351128084TG11GENIChomozygous119276411
45112808951128089A12GENIChomozygous128033707
45112810251128102C12GENIChomozygous128033708
45112810651128107G12GENIChomozygous128033709
45112810951128111GG13GENIChomozygous128033710
45112811151128112GA13GENIChomozygous119304574
45115771351157713G19GENIChomozygous128033737
45115955751159559TC9GENICheterozygous130929359
45115975251159752A18GENIChomozygous128033740
45115976651159766AGC18GENIChomozygous128033741
45116397851163978TC20GENIChomozygous128033742
45116398051163983GGG20GENIChomozygous128033743
45116398351163984GT20GENIChomozygous119276423
45116399051163990AT18GENIChomozygous128033744
45116399151163992CG18GENIChomozygous119621884
45114172551141726G8GENICheterozygous131640778
45115083751150838AG22GENICheterozygous131644184
45116397651163977GT20GENIChomozygous112649241
45117290651172907GT10GENIChomozygous112649262
45117291151172911T10GENIChomozygous128033747
45117291351172913G10GENIChomozygous128033748
45117292151172922CG10GENIChomozygous113022904
45117292451172925T11GENIChomozygous128033749
45117292951172930C12GENIChomozygous128033750
45117293051172931CG12GENIChomozygous119276425
45117293451172935AG12GENIChomozygous113022905
45117293751172937GTA13GENIChomozygous128033751