chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 90937217 90937218 A G 19 GENIC possibly homozygous 51738271 10 90939598 90939601 GGG --- 2 GENIC homozygous 51738277 10 90939820 90939821 G A 23 GENIC possibly homozygous 51738279 10 90940262 90940263 C T 4 GENIC homozygous 52996723 10 90941296 90941297 C A 11 GENIC homozygous 52996725 10 90941861 90941862 G A 14 GENIC possibly homozygous 52996727 10 90942630 90942631 A G 29 GENIC homozygous 52996729 10 90942865 90942866 C T 26 GENIC possibly homozygous 52996731 10 90943204 90943205 A G 17 GENIC homozygous 52165942 10 90943319 90943320 G GA 4 GENIC homozygous 51738291 10 90943385 90943386 T TGAG 10 GENIC homozygous 52165943 10 90943656 90943657 T C 15 GENIC homozygous 52996733 10 90943681 90943682 G A 17 GENIC possibly homozygous 52996735 10 90943829 90943830 G C 18 GENIC possibly homozygous 52996738 10 90943975 90943976 A G 26 GENIC possibly homozygous 52996740 10 90944249 90944250 A G 2 GENIC homozygous 52996742 10 90944372 90944373 C T 16 GENIC heterozygous 52996744 10 90944539 90944540 T C 13 GENIC homozygous 52996746 10 90944553 90944554 C T 5 GENIC homozygous 52996748 10 90946158 90946159 T C 29 GENIC homozygous 51538761 10 90949349 90949350 G GC 4 GENIC heterozygous 51738294 10 90953339 90953340 A G 3 GENIC homozygous 51738317 10 90955906 90955907 G C 9 GENIC heterozygous 52996750 10 90956392 90956394 CC -- 3 GENIC homozygous 51738319 10 90956505 90956506 T C 21 GENIC homozygous 51738323