chr start stop reference nuc variant nuc depth genic status zygosity variant ID 20 6611288 6611289 G GT 16 GENIC homozygous 732831256 20 6611372 6611373 A G 28 GENIC homozygous 607979188 20 6611464 6611465 A T 25 GENIC homozygous 607300837 20 6611465 6611466 A C 25 GENIC homozygous 607300838 20 6611597 6611602 TTTCG ----- 18 GENIC homozygous 732831257 20 6611688 6611689 T C 20 GENIC homozygous 607300839 20 6612400 6612401 G C 12 GENIC homozygous 607300840 20 6612770 6612771 G A 21 GENIC homozygous 607300841 20 6612996 6612997 C T 22 GENIC homozygous 607300842 20 6613051 6613052 A C 20 GENIC homozygous 607300843 20 6613073 6613080 AAAAAAC ------- 12 GENIC homozygous 732831258 20 6613120 6613121 A G 18 GENIC homozygous 607300844 20 6613534 6613535 C A 25 GENIC homozygous 607300845 20 6613555 6613556 A G 28 GENIC homozygous 607300846 20 6614651 6614652 C T 19 GENIC homozygous 607300847 20 6614840 6614844 ATTT ---- 21 GENIC homozygous 732831259 20 6614953 6614954 C A 4 GENIC heterozygous 607979189 20 6615189 6615190 C - 18 GENIC homozygous 732831260 20 6615265 6615266 A G 18 GENIC homozygous 607300848 20 6615381 6615382 G A 17 GENIC homozygous 607300849 20 6615453 6615454 C CA 15 GENIC homozygous 732831261