chr start stop reference nuc variant nuc depth genic status zygosity variant ID 20 6611288 6611289 G GT 29 GENIC homozygous 762563845 20 6611372 6611373 A G 15 GENIC homozygous 659214855 20 6611464 6611465 A T 21 GENIC homozygous 659214856 20 6611465 6611466 A C 22 GENIC homozygous 659214857 20 6611597 6611602 TTTCG ----- 26 GENIC homozygous 762563846 20 6611688 6611689 T C 16 GENIC homozygous 659214858 20 6612400 6612401 G C 53 GENIC homozygous 659214859 20 6612770 6612771 G A 34 GENIC homozygous 659214860 20 6612996 6612997 C T 34 GENIC homozygous 659214861 20 6613051 6613052 A C 25 GENIC homozygous 659214862 20 6613073 6613080 AAAAAAC ------- 14 GENIC heterozygous 762563847 20 6613120 6613121 A G 20 GENIC homozygous 659214863 20 6613534 6613535 C A 43 GENIC homozygous 659214864 20 6613555 6613556 A G 37 GENIC homozygous 659214865 20 6614651 6614652 C T 55 GENIC homozygous 659214866 20 6614840 6614844 ATTT ---- 34 GENIC homozygous 762563848 20 6615189 6615190 C - 34 GENIC homozygous 762563849 20 6615265 6615266 A G 51 GENIC homozygous 659214867 20 6615381 6615382 G A 44 GENIC homozygous 659214868 20 6615453 6615454 C CA 21 GENIC homozygous 762563850