chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID 8,40944463,40944464,A,AT,141,GENIC,heterozygous,707387203 8,40944715,40944716,G,-,83,GENIC,heterozygous,707387204 8,40944835,40944836,C,-,73,GENIC,heterozygous,707387205 8,40948264,40948265,T,-,77,GENIC,heterozygous,707387206 8,40950436,40950437,A,-,36,GENIC,heterozygous,707387207 8,40958441,40958442,T,-,40,GENIC,heterozygous,707387208 8,40960737,40960738,C,-,11,GENIC,heterozygous,707387209 8,40963805,40963806,C,CTTT,19,GENIC,heterozygous,707387212 8,40963806,40963808,TT,--,19,GENIC,heterozygous,707387210 8,40963807,40963808,T,-,19,GENIC,heterozygous,707387211 8,40966298,40966301,CTT,---,60,GENIC,heterozygous,707387213 8,40967667,40967668,A,-,19,GENIC,heterozygous,707387214 8,40968404,40968405,A,-,26,GENIC,homozygous,707387215 8,40969985,40969986,G,-,145,GENIC,heterozygous,707387216 8,40976084,40976085,T,-,29,GENIC,heterozygous,707387217 8,40980871,40980872,G,GT,9,GENIC,heterozygous,707387218 8,40980910,40980921,ATACAGGCCGA,-----------,43,GENIC,heterozygous,707387219 8,40982132,40982136,TGAT,----,37,GENIC,heterozygous,707387220 8,40982468,40982471,AAC,---,106,GENIC,heterozygous,707387221