chr start stop reference nuc variant nuc depth genic status zygosity variant ID 14 6174241 6174242 G A 16 GENIC homozygous 994924822 14 6174308 6174309 C T 12 GENIC homozygous 994924823 14 6174664 6174665 A C 22 GENIC homozygous 994924824 14 6174707 6174708 A G 15 GENIC homozygous 994924825 14 6174870 6174871 T G 16 GENIC homozygous 994924826 14 6175099 6175100 G C 25 GENIC homozygous 994924827 14 6176249 6176250 T C 21 GENIC homozygous 994924828 14 6176768 6176769 A T 22 GENIC homozygous 994924829 14 6177149 6177150 T C 30 GENIC homozygous 994924830 14 6177400 6177401 G C 25 GENIC homozygous 994924831 14 6177456 6177457 T C 36 GENIC homozygous 994924832 14 6177559 6177560 A G 26 GENIC homozygous 994924833 14 6177626 6177627 A G 31 GENIC homozygous 994924834 14 6181139 6181140 G A 23 GENIC homozygous 994924835 14 6217368 6217369 C T 29 GENIC homozygous 994924836 14 6217845 6217846 C T 23 GENIC homozygous 994924837 14 6217987 6217988 C T 19 GENIC homozygous 994924838 14 6218260 6218261 A G 23 GENIC homozygous 994924839 14 6218882 6218883 C G 18 GENIC homozygous 994924840 14 6219122 6219123 C T 22 GENIC homozygous 994924841 14 6219313 6219314 C T 19 GENIC homozygous 994924842 14 6220214 6220215 C G 18 GENIC homozygous 994924843 14 6220714 6220715 A G 23 GENIC homozygous 994924844