chr start stop reference nuc variant nuc depth genic status zygosity variant ID X 109806498 109806499 C A 32 GENIC homozygous 45593148 X 109806619 109806621 GT -- 26 GENIC heterozygous 45520520 X 109810264 109810265 A - 7 GENIC homozygous 45593150 X 109812542 109812543 A AT 14 GENIC homozygous 45193342 X 109816893 109816894 A G 24 GENIC homozygous 45193343 X 109817419 109817423 TGTG ---- 11 GENIC possibly homozygous 45593154 X 109824185 109824190 GAATA ----- 7 GENIC homozygous 45593156 X 109834298 109834299 C CAGTGGTAGAGCGCT 1 GENIC homozygous 45520524 X 109834305 109834306 C CTAGCAAGCA 2 GENIC homozygous 45520526 X 109840624 109840625 T - 20 GENIC heterozygous 45634314 X 109846126 109846127 G - 5 GENIC homozygous 45193344 X 109846139 109846140 A AT 7 GENIC homozygous 45193345 X 109846148 109846149 T - 9 GENIC homozygous 45193346 X 109864967 109864968 T TTGGGGATTTAGCTCAGTGGTAGAGCGCTTGCCTAGCAAG 4 GENIC homozygous 45520528 X 109869397 109869398 T TC 31 GENIC homozygous 45193348 X 109869494 109869495 T TC 21 GENIC homozygous 45193349 X 109831603 109831605 AT -- 13 GENIC heterozygous 45573058 X 109818269 109818271 GT -- 17 GENIC heterozygous 45573056