chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 46154590 46154591 A G 32 GENIC homozygous 51444202 10 46154908 46154909 A T 21 GENIC homozygous 51874917 10 46155760 46155761 C T 26 GENIC homozygous 51874919 10 46157313 46157314 T C 18 GENIC homozygous 51874922 10 46157742 46157743 T C 28 GENIC homozygous 51874925 10 46157999 46158000 C T 36 GENIC homozygous 51874928 10 46158275 46158276 G A 24 GENIC homozygous 51444207 10 46158502 46158503 T C 32 GENIC homozygous 51444208 10 46158511 46158512 T G 31 GENIC homozygous 51444209 10 46159445 46159446 A G 25 GENIC homozygous 51874931 10 46159503 46159504 C G 32 GENIC homozygous 51636700 10 46161264 46161265 A AC 17 GENIC homozygous 51636702 10 46163224 46163227 AAG --- 31 INTERGENIC homozygous 51444210 10 46164492 46164493 C T 20 INTERGENIC homozygous 51444211 10 46164526 46164527 A - 13 INTERGENIC possibly homozygous 51444212 10 46166767 46166768 T C 19 INTERGENIC homozygous 51444215 10 46166782 46166783 C G 18 INTERGENIC homozygous 51874934 10 46167048 46167049 A AG 19 INTERGENIC homozygous 51444216 10 46167208 46167209 G GGGGA 20 INTERGENIC homozygous 51444217 10 46167296 46167297 T C 34 INTERGENIC homozygous 51444218 10 46168328 46168329 A AGG 6 INTERGENIC homozygous 51874936 10 46170085 46170086 G A 27 INTERGENIC homozygous 51874939