chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID X,104720548,104720549,A,G,27,GENIC,homozygous,578035274 X,104721477,104721478,G,A,25,GENIC,homozygous,578035275 X,104723064,104723065,C,CTT,14,GENIC,homozygous,716853300 X,104723079,104723081,TT,--,7,GENIC,homozygous,716853301 X,104723788,104723789,A,G,24,GENIC,homozygous,578035276 X,104727044,104727045,A,-,15,GENIC,homozygous,716853302 X,104728161,104728162,G,-,28,GENIC,homozygous,716853303 X,104728227,104728228,C,T,28,GENIC,possibly homozygous,578035277 X,104730133,104730134,T,-,13,GENIC,homozygous,716853304 X,104730149,104730150,T,C,18,GENIC,homozygous,578035278 X,104731568,104731569,C,T,15,GENIC,homozygous,578035279 X,104733371,104733372,G,A,18,GENIC,homozygous,578035280 X,104734044,104734045,C,CT,7,GENIC,heterozygous,716853306 X,104734161,104734162,G,GC,28,GENIC,homozygous,716853307 X,104741856,104741857,G,GGTTT,15,GENIC,homozygous,716853308