chr start stop reference nuc variant nuc depth genic status zygosity variant ID 18 30859460 30859461 A T 40 GENIC possibly homozygous 796376462 18 30860373 30860374 T G 21 GENIC homozygous 796376463 18 30860433 30860434 A G 40 GENIC possibly homozygous 796376464 18 30936902 30936903 T G 27 GENIC homozygous 796376465 18 30937827 30937828 T G 15 GENIC homozygous 796376466 18 30953564 30953565 G T 40 GENIC possibly homozygous 796376467 18 30961539 30961540 T C 20 GENIC homozygous 796376468 18 30961541 30961542 A C 21 GENIC homozygous 796376469 18 30961570 30961571 T G 53 GENIC homozygous 796376470 18 30961830 30961831 C T 36 GENIC homozygous 796376471 18 30961993 30961994 C A 37 GENIC homozygous 796376472 18 30962305 30962306 G C 31 GENIC homozygous 796376473 18 30962333 30962334 T C 31 GENIC homozygous 796376474 18 30962348 30962349 C T 31 GENIC homozygous 796376475 18 30962397 30962398 T C 31 GENIC homozygous 796376476 18 30963381 30963382 C A 21 GENIC homozygous 796376477