chr start stop reference nuc variant nuc depth genic status zygosity variant ID 20 6611288 6611289 G GT 17 GENIC homozygous 770349864 20 6611372 6611373 A G 27 GENIC homozygous 673709848 20 6611464 6611465 A T 14 GENIC homozygous 673709849 20 6611465 6611466 A C 13 GENIC homozygous 673709850 20 6611597 6611602 TTTCG ----- 24 GENIC homozygous 770349865 20 6611688 6611689 T C 20 GENIC homozygous 673709851 20 6612400 6612401 G C 22 GENIC homozygous 673709852 20 6612770 6612771 G A 27 GENIC homozygous 673709853 20 6612996 6612997 C T 28 GENIC homozygous 673709854 20 6613051 6613052 A C 22 GENIC homozygous 673709855 20 6613073 6613080 AAAAAAC ------- 20 GENIC homozygous 770349866 20 6613120 6613121 A G 25 GENIC homozygous 673709856 20 6613534 6613535 C A 26 GENIC homozygous 673709857 20 6613555 6613556 A G 25 GENIC homozygous 673709858 20 6614651 6614652 C T 20 GENIC homozygous 673709859 20 6614840 6614844 ATTT ---- 25 GENIC homozygous 770349867 20 6614953 6614954 C A 4 GENIC homozygous 673709860 20 6615189 6615190 C - 29 GENIC homozygous 770349868 20 6615265 6615266 A G 16 GENIC homozygous 673709861 20 6615381 6615382 G A 24 GENIC homozygous 673709862 20 6615453 6615454 C CA 20 GENIC homozygous 770349869