chr start stop reference nuc variant nuc depth genic status zygosity variant ID 20 6611288 6611289 G GT 14 GENIC homozygous 758030045 20 6611372 6611373 A G 22 GENIC homozygous 651618728 20 6611464 6611465 A T 11 GENIC homozygous 651618729 20 6611465 6611466 A C 12 GENIC homozygous 651618730 20 6611597 6611602 TTTCG ----- 18 GENIC homozygous 758030046 20 6611688 6611689 T C 17 GENIC homozygous 651618731 20 6612400 6612401 G C 17 GENIC homozygous 651618732 20 6612770 6612771 G A 21 GENIC homozygous 651618733 20 6612996 6612997 C T 18 GENIC homozygous 651618734 20 6613051 6613052 A C 10 GENIC homozygous 651618735 20 6613073 6613080 AAAAAAC ------- 12 GENIC possibly homozygous 758030047 20 6613120 6613121 A G 15 GENIC homozygous 651618736 20 6613534 6613535 C A 16 GENIC homozygous 651618737 20 6613555 6613556 A G 23 GENIC homozygous 651618738 20 6614651 6614652 C T 22 GENIC homozygous 651618739 20 6614840 6614844 ATTT ---- 6 GENIC homozygous 758030048 20 6614953 6614954 C A 1 GENIC homozygous 651618740 20 6615189 6615190 C - 19 GENIC homozygous 758030049 20 6615265 6615266 A G 13 GENIC homozygous 651618741 20 6615381 6615382 G A 13 GENIC homozygous 651618742 20 6615453 6615454 C CA 16 GENIC homozygous 758030050