chr start stop reference nuc variant nuc depth genic status zygosity variant ID 8 116730972 116730973 G A 37 INTERGENIC homozygous 53305900 8 116730989 116730990 C CCT 23 INTERGENIC homozygous 53291274 8 116731185 116731186 A G 24 INTERGENIC homozygous 53291276 8 116731395 116731396 T C 28 INTERGENIC homozygous 53291277 8 116732796 116732797 C T 22 GENIC homozygous 53305901 8 116734979 116734980 G GT 13 GENIC heterozygous 52828606 8 116735948 116735949 G A 19 GENIC homozygous 53305902 8 116735982 116735983 G A 16 GENIC homozygous 53305903 8 116737670 116737671 A C 18 GENIC homozygous 53291279 8 116738469 116738483 ACATGTGTTATCAG -------------- 7 GENIC homozygous 53305904 8 116739379 116739380 C T 16 GENIC homozygous 53305905 8 116739403 116739404 C CT 3 GENIC heterozygous 52828608 8 116739880 116739881 C T 28 GENIC possibly homozygous 53305906 8 116740060 116740061 A G 25 GENIC homozygous 53291282 8 116740295 116740296 C A 32 GENIC homozygous 52828610 8 116740619 116740620 G GA 11 GENIC homozygous 53291283 8 116740646 116740650 GTGA ---- 9 GENIC homozygous 53291284 8 116741370 116741371 C T 43 GENIC possibly homozygous 53305907 8 116741509 116741510 A - 22 GENIC homozygous 53291285 8 116742162 116742163 G A 21 GENIC homozygous 53305908 8 116743422 116743423 G A 20 GENIC homozygous 53305909 8 116743546 116743547 G A 24 GENIC homozygous 53291290 8 116743849 116743850 C T 27 GENIC homozygous 53305910 8 116743998 116743999 G A 19 GENIC homozygous 53305911 8 116744759 116744760 A G 15 GENIC homozygous 53291291 8 116745301 116745302 C T 15 GENIC homozygous 53305912 8 116746424 116746427 AAA --- 13 GENIC homozygous 53291293 8 116746722 116746723 T TC 29 GENIC homozygous 53305913 8 116747104 116747105 G C 14 GENIC homozygous 53305914 8 116749878 116749879 T - 4 GENIC heterozygous 53291296 8 116750367 116750368 G A 17 GENIC homozygous 53305915