chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124905054349050544AC2GENICheterozygous50230922
124905139449051395CA27GENIChomozygous50230926
124905230049052301AAGT4GENICheterozygous50230930
124905236449052365AT17GENIChomozygous50230932
124905276849052769TC21GENIChomozygous50230934
124905539549055396AC22GENICpossibly homozygous50230936
124905572249055723TG6GENIChomozygous50513695
124905593049055933AAG---3GENIChomozygous50513697
124905614649056147CA9GENIChomozygous50230942