chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7143108980143108981A15GENIChomozygous131025954
7143109529143109530GT11GENIChomozygous115942857
7143111868143111869AT19GENICheterozygous115942860
7143111874143111875GA20GENICheterozygous115942861
7143111901143111902GA19GENIChomozygous115942862
7143112573143112574AG16GENIChomozygous115942863
7143112607143112608CG16GENIChomozygous115942864
7143112736143112737CG12GENIChomozygous115942866
7143112753143112754CT16GENIChomozygous115942867
7143112769143112770TA17GENIChomozygous115942868
7143112448143112448C8GENIChomozygous128530896
7143109803143109804AG2GENIChomozygous131882905
7143110028143110029GA10GENIChomozygous116233223
7143110046143110047GA7GENIChomozygous116396793
7143110713143110714GA10GENIChomozygous116099268
7143112965143112966CG29GENIChomozygous116099272