chr start stop reference nuc variant nuc depth genic status zygosity variant ID 12 49330656 49330657 T C 17 GENIC homozygous 986060738 12 49330802 49330803 T C 7 GENIC homozygous 986060739 12 49331002 49331003 G A 12 GENIC homozygous 986060740 12 49331099 49331100 A C 19 GENIC homozygous 986060741 12 49331242 49331243 T C 20 GENIC homozygous 986060742 12 49331924 49331925 C T 16 GENIC homozygous 986060743 12 49332445 49332446 C T 7 GENIC homozygous 986060744 12 49333270 49333271 A C 7 GENIC homozygous 986060745 12 49333996 49333997 A G 9 GENIC homozygous 986060746 12 49334432 49334433 C G 14 GENIC homozygous 986060747 12 49334857 49334858 G A 14 GENIC homozygous 986060748 12 49335350 49335351 T G 16 GENIC homozygous 986060749 12 49337448 49337449 A G 26 GENIC homozygous 986060750 12 49338137 49338138 G T 18 GENIC homozygous 986060751 12 49339394 49339395 G C 9 GENIC homozygous 986060752 12 49339446 49339447 C G 7 GENIC homozygous 986060753 12 49340050 49340051 T C 9 GENIC homozygous 986060754 12 49341210 49341211 C T 12 GENIC homozygous 986060755 12 49358877 49358878 A G 8 GENIC homozygous 986060756 12 49369810 49369811 G A 17 GENIC homozygous 986060757 12 49370024 49370025 C T 8 GENIC homozygous 986060758 12 49372606 49372607 G A 18 GENIC homozygous 986060759 12 49373017 49373018 A G 12 GENIC homozygous 986060760 12 49386849 49386850 A G 16 GENIC homozygous 986060761 12 49394909 49394910 G A 8 GENIC homozygous 986060762