chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
144417005544170056GC17GENIChomozygous139527738
144417013144170132CG17GENIChomozygous139527740
144417057644170577TC11GENIChomozygous148361123
144417099144170992CT22GENIChomozygous148361124
144417106644171067AG21GENIChomozygous139527741
144417127344171274AT12GENICheterozygous403359117
144417340844173409TC18GENICpossibly homozygous148361125
144417402544174026AT17GENIChomozygous148361126
144417340844173409TA18GENICheterozygous403741528
144417524144175241CAGCGAGTTAGA13GENIChomozygous139396237
144417777444177775CT14GENIChomozygous148361127
144418151644181516A13GENICpossibly homozygous146264197
144418304844183049AG15GENIChomozygous139527749
144418777144187772GA19GENIChomozygous139527752
144419041944190420A8GENICheterozygous141043425
144419150144191502AT13GENIChomozygous148361128
144419792844197929A13GENIChomozygous148354940
144419246944192470GC11GENIChomozygous148361129
144419508444195085GA10GENIChomozygous148361130
144417724544177247AT16GENIChomozygous148354937
144419367044193670T9GENIChomozygous148354939
144419919344199203TCAGCCATAA20GENICpossibly homozygous148354941