chr start stop reference nuc variant nuc depth genic status zygosity variant ID 16 20531098 20531099 A C 13 GENIC homozygous 47327908 16 20531592 20531593 A G 27 GENIC possibly homozygous 48089357 16 20531619 20531620 A G 26 GENIC possibly homozygous 48089358 16 20531637 20531638 A AC 25 GENIC possibly homozygous 48089359 16 20531999 20532000 T A 18 GENIC homozygous 47740650 16 20532055 20532056 C A 17 GENIC possibly homozygous 48089360 16 20532943 20532944 A G 13 GENIC homozygous 47327912 16 20533104 20533105 T C 17 GENIC homozygous 48089361 16 20534167 20534168 G A 26 GENIC possibly homozygous 48089362 16 20534220 20534221 G A 19 GENIC possibly homozygous 48089363 16 20534590 20534591 C T 19 GENIC possibly homozygous 48089364 16 20534855 20534856 C - 13 GENIC homozygous 47327916 16 20536467 20536468 G A 36 GENIC homozygous 48089365 16 20536650 20536651 A G 28 GENIC possibly homozygous 48089366 16 20536951 20536952 A AAT 16 GENIC homozygous 48089367 16 20536975 20536976 A G 21 GENIC homozygous 48089368 16 20537161 20537162 G T 25 GENIC homozygous 48089369 16 20538465 20538466 T C 13 GENIC homozygous 47327921 16 20538520 20538521 T C 20 GENIC possibly homozygous 47327923 16 20538532 20538533 T TAG 23 GENIC possibly homozygous 47327925 16 20539046 20539047 G T 15 GENIC homozygous 47327927 16 20540560 20540562 TG -- 27 GENIC homozygous 47327929 16 20541582 20541583 G A 6 GENIC homozygous 47327931