chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
91543313715433138CT30GENICpossibly homozygous142132303
91543446115434461GA25GENIChomozygous142109824
91543541915435420CG35GENIChomozygous142132304
91543608015436080C37GENIChomozygous142109825
91543692815436929AC56GENIChomozygous142132305
91543754615437547AG49GENIChomozygous142132306
91543790515437906TC55GENICheterozygous138523173
91543785615437857GA54GENICheterozygous138523168
91543785815437859GA55GENICheterozygous138523169
91543786515437866CG57GENICheterozygous138523170
91543786815437869CT54GENICheterozygous138523171
91543789515437896GA53GENICheterozygous138523172
91543788915437889A49GENICheterozygous138448728
91543791515437916GA54GENICheterozygous138523174
91543793315437934GA53GENICheterozygous138523175
91543786415437865TC56GENICheterozygous403259383
91543795215437953GA52GENICheterozygous403259384