chr start stop reference nuc variant nuc depth genic status zygosity variant ID 14 6174241 6174242 G A 8 GENIC homozygous 950775616 14 6174308 6174309 C T 10 GENIC homozygous 950775617 14 6174664 6174665 A C 18 GENIC homozygous 950775618 14 6174707 6174708 A G 18 GENIC homozygous 950775619 14 6175099 6175100 G C 21 GENIC homozygous 950775620 14 6176249 6176250 T C 15 GENIC homozygous 950775621 14 6176768 6176769 A T 25 GENIC homozygous 950775622 14 6177149 6177150 T C 28 GENIC homozygous 950775623 14 6177400 6177401 G C 20 GENIC homozygous 950775624 14 6177456 6177457 T C 31 GENIC homozygous 950775625 14 6177559 6177560 A G 25 GENIC homozygous 950775626 14 6177626 6177627 A G 21 GENIC homozygous 950775627 14 6177826 6177827 A G 25 GENIC homozygous 950775628 14 6217368 6217369 C T 24 GENIC homozygous 950775629 14 6217987 6217988 C T 23 GENIC homozygous 950775630 14 6218882 6218883 C G 18 GENIC homozygous 950775631 14 6219122 6219123 C T 12 GENIC homozygous 950775632 14 6219313 6219314 C T 28 GENIC homozygous 950775633 14 6220214 6220215 C G 16 GENIC homozygous 950775634 14 6220714 6220715 A G 24 GENIC homozygous 950775635