chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID 1,44313659,44313660,C,CTGCT,3,GENIC,homozygous,740947066 1,44313662,44313666,ATGA,----,3,GENIC,homozygous,740947067 1,44313723,44313724,A,AGTGCGCG,4,GENIC,homozygous,740947068 1,44313725,44313728,CAA,---,4,GENIC,homozygous,740947070 1,44313729,44313730,C,T,4,GENIC,homozygous,616258834 1,44313731,44313732,G,GC,4,GENIC,homozygous,740947071 1,44313733,44313734,T,TTA,4,GENIC,homozygous,740947072 1,44313735,44313736,T,TGGTG,4,GENIC,homozygous,740947073 1,44313863,44313864,T,C,23,GENIC,homozygous,616258835 1,44313868,44313869,A,C,26,GENIC,homozygous,616258836 1,44313875,44313876,T,TTA,29,GENIC,homozygous,740947074 1,44313878,44313879,G,A,31,GENIC,homozygous,616258837 1,44313880,44313881,A,T,32,GENIC,homozygous,616258838 1,44313884,44313888,TCAT,----,35,GENIC,homozygous,740947075 1,44313912,44313913,C,T,38,GENIC,homozygous,616258839 1,44313919,44313926,CCCTTGT,-------,39,GENIC,homozygous,740947076 1,44313952,44313953,G,T,28,GENIC,homozygous,616258840 1,44313963,44313964,G,T,29,GENIC,homozygous,616258841