chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124347380443473805CT42GENIChomozygous50211911
124347462043474621CCCA37GENIChomozygous50211912
124347466843474669CA44GENIChomozygous50211913
124347501843475019A-19GENICpossibly homozygous50329926
124347619543476196TC21GENIChomozygous50211915
124347642643476427TC42GENIChomozygous50211916
124347863043478631GGCA1GENIChomozygous50211917
124347879743478803GCGCGC------15GENIChomozygous50211918
124347880743478808GA25GENICheterozygous50211919
124347880943478816GCGCGCG-------20GENICheterozygous50211920
124347882543478827GC--21GENICheterozygous50211921
124347882643478827CCGT8GENICheterozygous50211922
124348008943480090AG33GENIChomozygous50211924